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Toxin Rid

Introduction

Are you worried about a recent indulgence in weed potentially affecting your job prospects due to a mandatory drug test? Well, fret not, because there might be a solution for you – Toxin Rid. In this review, we’ll delve into the world of Toxin Rid, a detox product designed to help you pass urine drug tests with ease.

Toxin Rid is a detoxification product specifically tailored for those facing urine drug tests, especially after enjoying some recreational marijuana. In our fast-paced lives, stress can push some of us to seek relaxation through substances like pot. However, this choice comes with consequences, particularly in the professional realm, where drug screenings are increasingly common. Even in states where cannabis is legal, potential employees testing positive for drugs may find their job opportunities slipping away.

Now, let’s talk about Toxin Rid and its significance. Drug tests can detect residues in your body for up to three months, posing a significant challenge. But fear not – Toxin Rid offers a potential solution. This cleansing detox product aims to prevent the detection of THC during screenings, providing an option to maintain your job or secure that dream position.

Product Description

Are you stressed about passing a drug test after enjoying some pot over the weekend? Well, here’s a solution for you – Toxin Rid. In this Toxin Rid review, we’ll break down the details in a simple way. First off, Toxin Rid is a detox product designed to help you pass urine drug tests. It comes in different programs, like 3-day, 5-day, and 10-day detox plans.

Now, let’s talk about the manufacturer. Toxin Rid is made by a company with a solid background and achievements, ensuring the product’s credibility. Why is this important? Well, many jobs these days test for drugs, and failing such tests can jeopardize your employment opportunities. Toxin Rid helps you avoid this by flushing out drug residues from your body. It contains natural ingredients, like vitamins and herbs, which accelerate the body’s natural detox process. The detox formula comes in pill form, and you can choose a program based on your weed-smoking habits – whether you’re a heavy, moderate, or light smoker.

The working mechanism is simple – Toxin Rid aids your body in getting rid of drug metabolites through urine and feces, ensuring a negative result in drug tests.

If you’re curious about firsthand experiences with Toxin Rid, check out this review on https://www.mid-day.com/lifestyle/infotainment/article/toxin-rid-product-line-review-detox-for-every-drug-test-type-23313778. The article provides valuable insights into the product’s effectiveness and user satisfaction, complementing our detailed breakdown.

Ingredients and their Functions

In the Toxin Rid review, understanding the ingredients and how they function is crucial. This detox product is designed to help individuals pass urine drug tests, especially if they’ve used cannabis. Let’s dive into the ingredients and their roles.

To begin with, Toxin Rid contains key elements that contribute to its detoxification process. These include Kelp, Iron, Boron, Calcium, Magnesium, Chloride, Sodium, Potassium, and Alfalfa leaf extract. Additionally, the formula includes a fiber supplement with Dietary Fiber and Psyllium Husk Powder, along with a detox liquid containing Chloride, Potassium, Boron, Sodium, Lithium, Sulfate, and Magnesium.

Each ingredient plays a vital role in the detoxification process. For instance, activated charcoal, a common detox ingredient, is absent here. Instead, Toxin Rid relies on natural components like Kelp, known for its rich mineral content, and Alfalfa leaf extract, recognized for its detox properties. The dietary fiber supplement aids in toxin absorption, ensuring effective elimination through feces.

Understanding the significance of these ingredients is crucial. Activated charcoal, often found in detox products, is known for its toxin absorption capabilities. In Toxin Rid, the absence of activated charcoal is compensated by the inclusion of elements like Kelp, contributing to a natural and effective detox process.

Herbal components, another essential aspect, play a role in liver support. While some detox products use synthetic or harsh chemicals, Toxin Rid opts for natural ingredients like Alfalfa leaf extract, promoting a gentle yet effective detoxification.

Toxin Rid’s ingredients work harmoniously to support a natural detoxification process. For individuals facing drug tests, understanding the functions of these elements provides confidence in the product’s efficacy. Whether you’re a regular or occasional weed user, Toxin Rid’s diverse ingredients cater to various needs, making it a promising option for those seeking a reliable detox solution.

How to Use Toxin Rid

Toxin Rid is a detox product designed to help individuals pass urine drug tests, especially for those who have used marijuana. Drug tests can detect traces of drug residues in the body for up to 90 days, making it crucial to find an effective solution. Toxin Rid offers a step-by-step guide on how to use their product, including dosage instructions for different programs and tips for maximizing effectiveness.

The Toxin Rid program is available in various durations, ranging from 1 to 10 days, allowing users to choose based on their level of marijuana consumption. The product consists of pills, a detox liquid, and optional dietary fiber. The detox process involves natural ingredients like vitamins, herbs, and minerals, such as kelp, iron, boron, calcium, magnesium, chloride, sodium, potassium, and alfalfa leaf extract. These ingredients work together to expedite the body’s natural detoxification process.

For a 10-day Toxin Rid program, users are advised to abstain from toxins for the first 24 hours and start taking three pills every 5 hours for the next 9 days. Maintaining a healthy diet, staying hydrated with water and juice, and avoiding greasy foods are recommended during the detox period. On the 10th day, users are instructed to consume a detox drink with water and dietary fiber before the test, ensuring a thorough detoxification process.

Toxin Rid claims to work effectively by providing electrolytes that help beat urine drug tests, and its main ingredients, including alfalfa, kelp, and boron, are known for their detoxifying properties. Users are encouraged to follow the provided instructions carefully to increase the chances of passing the drug test with confidence.

Pros and Cons

Toxin Rid is a popular detox product designed to help individuals pass urine drug tests, especially for those who have indulged in marijuana use. Let’s explore the pros and cons of Toxin Rid based on customer feedback.

Starting with the positive aspects, many users have reported the effectiveness of Toxin Rid in detoxifying their bodies. The product seems to be easy to use, with customers praising its convenience. Additionally, some users claim potential fast results, which can be crucial when facing a looming drug test.

On the flip side, there are some drawbacks mentioned by users. First, the taste or palatability of Toxin Rid may not be favorable for everyone. Some users also highlight the price considerations, as Toxin Rid is reported to be relatively expensive compared to similar detox products in the market. Another point of consideration is the individual variations in results, implying that the effectiveness of Toxin Rid may vary from person to person.

Toxin Rid appears to have its advantages, including effectiveness in detoxifying, ease of use, and potential fast results. However, users should be mindful of the taste, price, and individual differences in results when considering this product. It’s essential to weigh the pros and cons based on your specific needs and circumstances, especially if you are seeking a reliable solution to pass a urine drug test.

Customer Feedback

In examining the Toxin Rid detox product, one crucial aspect to consider is customer feedback. This section involves gathering and summarizing reviews from individuals who have used Toxin Rid to pass urine drug tests. Customer reviews serve as valuable insights into the product’s effectiveness and potential concerns.

To begin, users consistently praise Toxin Rid for its positive impact on drug test results. Common themes in positive feedback highlight successful outcomes in beating drug tests, with users sharing their experiences of passing tests after following the recommended detox programs. The effectiveness of Toxin Rid in various types of drug tests, such as urine, saliva, and hair follicle tests, is frequently mentioned.

On the flip side, there are also common concerns and criticisms expressed by some users. Negative reviews often revolve around issues like the product’s relatively higher cost compared to alternatives, potential side effects such as diarrhea, and the lack of a 100% guarantee of effectiveness. Users emphasize the importance of understanding one’s usage pattern, with heavy cannabis users occasionally needing additional detox packages.

These customer reviews provide valuable insights for potential users of Toxin Rid, allowing them to weigh the product’s pros and cons before making a decision.

It’s crucial for individuals to consider their own usage patterns and the specific detox program duration suitable for their needs, whether it’s a 1-day, 5-day, or 10-day program.

Q&A Section

Q: Can the lab tester find out if I have used Toxin Rid?

A: No, the pills are not detectable by the lab tester. However, it is crucial to keep the product away from the testing lab to avoid any unnecessary problems.

Q: Does Toxin Rid work to beat alcohol drug tests?

A: Yes, it can help beat alcohol drug tests, but it’s important to abstain from consuming alcohol on the day of the test due to the small detection window.

Q: How long does the effect of Toxin Rid last?

A: The duration of the effect depends on the detox program chosen and the type of weed user you are. The manufacturer claims an infinite duration, but in practical terms, the effect lasts up to five hours. To maintain the effect, a new detox program is needed upon resuming cannabis use.

Q: Does Toxin Rid help flush out traces of opiates?

A: Yes, it can help flush out traces of opiates, especially when combined with vitamin B and creatinine supplements. These supplements should be taken on the day of the test.

Q: Where can I get Toxin Rid detox?

A: Unfortunately, Toxin Rid is not available at local stores or online retailers like Amazon. To make a purchase, you have to order it directly from the manufacturer.

Q: Is it possible to pass drug tests with Toxin Rid in just one day?

A: Yes, it is possible. Toxin Rid offers a 1-day detox program for the fastest detoxification process to beat drug tests.

Summing Up

In conclusion, Toxin Rid is a popular detox product designed to help individuals pass urine drug tests, particularly for those who have used marijuana. The fast-paced nature of our lives can lead some to use cannabis as a way to de-stress, but the consequences, especially in employment situations, can be significant due to routine drug testing by employers. Toxin Rid offers a solution by providing a range of detox programs, with options lasting from 1 to 10 days, depending on individual needs and usage patterns.

The detox pills, containing ingredients like kelp, iron, and magnesium, aim to accelerate the body’s natural detoxification process, ensuring the removal of drug metabolites within a shorter timeframe. Toxin Rid is considered a reliable option for those seeking a natural detoxification process, avoiding the potential pitfalls of synthetic urine or harsh detox methods for hair follicle tests. The detox program also includes dietary recommendations, emphasizing a healthy diet routine, hydration, and avoiding certain foods to enhance effectiveness.

The review emphasizes the importance of following the Toxin Rid instructions meticulously, particularly during the chosen detox program’s duration. This includes refraining from toxin intake on the first day, taking the prescribed number of pills each day, and following a specific routine on the testing day, involving a detox drink and dietary fiber. Toxin Rid claims to work for various drug tests, including saliva, urine, blood, and even alcohol tests, providing a comprehensive solution for individuals facing different testing scenarios.

While positive customer reviews highlight Toxin Rid’s effectiveness in helping users pass drug tests successfully, negative reviews also caution about individual variations and the need to understand one’s usage patterns. Additionally, the article addresses the product’s cost, potential side effects like diarrhea, and the lack of FDA approval, relying instead on third-party testing for authenticity.

Toxin Rid appears to be a viable option for those seeking a reliable and natural detox solution, but potential users are urged to be aware of their state’s laws regarding detox products and to make an informed decision based on individual circumstances.

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Drug Testing

Ultra Pure Synthetic Urine: Your Gateway to Passing Drug Test

Before we talk about Ultra Pure Synthetic Urine, there are currently three primary methods for drug testing prevalence. While the other two are hair and saliva, the urine test is number one. In the U.S., almost 90% of companies choose to go the urine route when it comes to drug testing, according to research by SHRM.

That’s because urine lasts the longest when it comes to drug or alcohol retention. While saliva lasts as long as 12 hours, urine still holds in the toxin for up to 72 hours for heavy users. It is also why most heavy users fail the urine test. But that doesn’t mean everyone does.

According to multiple anonymous studies, even heavy users can pass DOT or non-DOT drug and alcohol tests using Ultra Pure Synthetic Urine. Also known as fake pee, it has all the ingredients and constituents that enable it to aid in your drug tests.

However, there are some things you’ll need to know first, and that’s the essence of this article. In this guide, we’ll go over the product, the Ultra Pure Synthetic Urine ingredients, and the step-by-step guide to how to use the product.

Ultra Pure Synthetic Urine

Ultra Pure Synthetic Urine Main Features

Ultra Klean Synthetic Urine is a high-quality, non-biological solution that precisely mimics human urine. With a homogeneous composition containing essential elements like uric acid, specific gravity, and creatinine, it stands out for its accuracy in replicating natural urine.

What makes Ultra Pure unique is its commitment to precision. Unlike other synthetic urine products, Ultra Pure Fake Pee precisely matches the chemical composition of real urine, ensuring reliable success in even the most stringent drug tests.

Crafted with advanced laboratory techniques, Ultra Pure’s formula remains undetectable by standard drug testing methods. Packaged in a convenient 2-ounce liquid form, it is easy to use and transport, providing a ready solution for various testing scenarios.

Key Features:

  • Non-biological, Homogeneous Formula: Ensures consistency and reliability.
  • Accurate Imitation of Human Urine Composition: Reflects natural urine components.
  • Undetectable by Standard Drug Testing Methods: A foolproof solution.
  • Convenient Liquid Form: User-friendly and easily transportable.
  • 2-Ounce Volume: Ample supply for varied testing situations.

In conclusion, Ultra Pure Synthetic Urine stands as the top choice for urinalysis, offering unmatched quality, precision, and practicality. It provides a reliable solution for individuals aiming to confidently navigate drug tests.

How to Pass a Urine Drug Test with Ultra Pure Synthetic Urine?

Customers should follow the following steps on how to use Ultra Pure synthetic urine:

STEP I
Open the kit and remove the cap to unseal it. If the cap feels loose, return it.

STEP II
Microwave the opened kit for about ten seconds only.

STEP III
After heating, cap the bottle and shake its contents together. Watch the temperature strip; it should be between 90°and 99°F.

STEP IV
Repeat for about 5 seconds if not. If the temperature strip reads nothing, or it appears too hot, allow the bottle to cool down and read again.

STEP V
Place the heating pad in between the bottle and the belt and attach the bottle to your thigh or pelvic region. Ensure the bottle is positioned cap-down and the heating pad is gracing the fabric of your cloth and NOT YOUR SKIN.

STEP VI
Walk into your DOT or non-DOT test and pour out the fake pee.

Pee temperature for drug test

Tips and Precautions for Optimal Results

  • Check the temperature once more, before you go into the test. The correct temperature (94-99°) is the most important thing needed to pass the test.
  • Heat your bottle at most 8 hours before your test. Don’t heat it the day before.
  • Open the bottle only on the day of the test. Opening it before the day can tamper with the biological makeup of the pee.
  • For the best results, do not smoke or drink any toxin substance at least 24-48 hours before your test.

Ultra Pure Synthetic Urine Reviews

While we can go on about the benefits of the product, an Ultra Pure Synthetic Urine review would be a lot more convincing. Here are some testimonials:

Comment
by from discussion
indrugtesthelp

The customer used Ultra Klean for a 10-panel test in the UK. Ordered two weeks before the test, warmed the urine, and passed with flying colours at 34°C. Effective, but advise caution with overheating and strategic timing.

Comment
byu/EggRepresentative857 from discussion
indrugtesthelp

Ultra Klean’s Ultra Pure Synthetic Urine is a lifesaver for this user! It worked 100% for both lab and home testing, saving the day in a crucial moment.

Comment
byu/outtathedamnway from discussion
inStonerProTips

The user has had consistent success with Ultra Klean’s Ultra Pure Synthetic Urine. He mentions it’s pre-mixed, reliable, and comes in a distinctive bright yellow box.

Where to Buy Ultra Pure Fake Urine?

The subject of where to purchase this product is not straightforward because not all states allow the purchase of fake pee. According to a 2018 publication in the Washington Post, Indiana and New Hampshire banned the sale, purchase, and use of the product. Other publications have confirmed that other states like Oklahoma, Louisiana, Arkansas, New Michigan, Alabama, Arizona, Missouri, Mississippi, Kansas, Georgia, Florida, and up to six other states have also banned its use. Therefore, it’s recommended to do your findings and ensure that Ultra Pure Synthetic Urine isn’t illegal in your state.

If you have researched and can order the product, then there are three ways to buy fake pee.

  1. Through the official website: Go to the Ultra Klean official website and purchase the product there. It’s risk-free and more reliable, and it comes with added benefits.
  2. Through Google: Though this is not reliable at all, you can simply type ‘Ultra Pure Synthetic Urine near me’ on the search bar, and that would present you with multiple online vendors to buy from. Some of them could include Walgreens and other local retailers.
  3. Through Amazon: Getting an Ultra Pure Synthetic Urine Amazon product is more reliable than the first option, but it’s still not the most recommended.

How Much Does It Cost?

The Ultra Klean fake pee comes in three sizes: The 2oz which is $34.95, the 4oz ($41.95), and the complete kit ($72.95). Buying the single pieces might seem cheaper, but since the belt alone can cost between 40-50 dollars and the heating pad is about $3, you’ll save between $8 and $20 by buying the complete kit.

Pros and Cons

Below are the advantages and limitations of the Ultra Klean Synthetic Urine

Pros Cons
  • Ultra Pure Synthetic Urine is easy to find in multiple online stores and local retail shops.
  • The product has a high success potential with multiple positive reviews.
  • It is easy to use and heat up.
  • The pee stays warm for up to 8 hours which is great for those who have first to do a physical test.
  • The company has been established for over 12 years. Hence it is reliable.
  • Due to its high potential for success, it costs more than some other alternatives.
  • Without the right temperature, there’s a tendency for a failed test.

What Additional Products Can Be Used with Ultra Pure Synthetic Urine?

In the complete kit, all these additional products are already added. They include:

  • The Urine Itself: It comes in a bottle of either 2oz or 4oz.
  • Heating pads: These are what you should use to keep the bottle warm until your test.
  • Special Belt: The belt is what keeps the bottle attached to your thigh or pelvic region and under your clothes.
  • Ultra Klean Cleanse: The cleanser is the detox for your hair. You are to use it as a shampoo and conditioning hair detoxing product.
  • Ultra Klean Wash: The wash is to rinse your mouth before the test to get your saliva rid of toxins.

Note that you must practice at home before heading over to your test. A day or two days before your test, purchase the product and practice pouring the capped content into a cup. Learn how to attach the belt and do this about 3 to 5 times.

Ultra Pure Synthetic Urine vs UPass Urine

You might mistake our product of the day for another product called UPass Urine. These brands might have the same products, but they are not the same. The table below compares the two:

Variable Ultra Pure Fake Pee UPass Urine
Features The urine, hair cleanser, mouthwash, belt, heating pad, and instructions. The urine, hand warmer, rubber band, and instructions.
Ingredients Creatinine, uric acid, distilled water, etc. Creatinine, vitamins, and many others.
Form Liquid Liquid
Temperature Control 8 hours 6 hours
Effectiveness 5 out of 5 4 out of 5
Price $34.95 $29.95
Ease of Use Open-heatup-shake-attach Open-heatup-shake-attach
Discreetness Very discreet Very discreet

Q&A

What Sets Ultra Pure Synthetic Urine Apart From Its Counterparts?

Ultra Pure distinguishes itself by precisely replicating the chemical composition of human urine, ensuring unparalleled accuracy in successfully passing drug tests.

How Does Ultra Pure Achieve Invisibility in Standard Drug Tests?

Through advanced techniques and a distinct formula, Ultra Pure duplicates the properties of real urine, rendering it nearly indistinguishable during testing.

Is Ultra Pure Suitable for Various Types of Drug Tests?

It’s designed to be versatile and effective across a range of urinalysis scenarios.

Why are Components Like Uric Acid and Creatinine Crucial in Ultra Pure Synthetic Urine?

These components mirror those in natural urine, enhancing Ultra Pure’s effectiveness in successfully passing drug tests.

What Makes the Liquid Form of Ultra Pure Synthetic Urine User-Friendly?

Packaged conveniently in a 2-ounce volume, the liquid form is easily dispensed and transported, making it the preferred choice for straightforward and trouble-free drug testing solutions.

Conclusion

Ultra Pure Synthetic Urine by Ultra Klean (existing for 12 years+) combined a mixture of distilled water, urea, uric acid, and other essential components to meet the pH level, temperature, volume, specific gravity, and creatinine level of actual pee. With this manufacturing process, the Ultra Pure synthetic pee has become one of the most trusted products for simulating real urine. In conclusion, this product is easy to use and also has a very impressive success rate.

Read more interesting information on our website!

References

  • Official website:
    www.ultrakleanurine.com/
  • Roy Maurer (2018, February 15). Hair, Saliva or Urine—Which Is Best for Drug-Testing Job Candidates
    https://www.shrm.org/resourcesandtools/hr-topics/talent-acquisition/pages/hair-saliva-urine-drug-testing-methods-specimens.aspx
  • Crumpton SD, Sutheimer CA. Specimen adulteration and substitution in workplace drug testing. Forensic Sci Rev. 2007;19(1–2):1–27.
    https://pubmed.ncbi.nlm.nih.gov/26247281/
  • American Addiction Centers Editorial Staff (Jan 19, 2023). States Move to Ban Synthetic Urine.
    https://drugabuse.com/blog/states-move-to-ban-synthetic-urine/
  • Phan HM, Yoshizuka K, Murry DJ, Perry PJ. Drug testing in the workplace. Pharmacotherapy. 2012;32(7):649–56.
    https://pubmed.ncbi.nlm.nih.gov/22605533/
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MedPointe Enforces Patent Surrounding Cough-Cold Product

COMPANY VIGOROUSLY DEFENDS ITS TUSSI-12®D TABLETS AND TUSSI-12®DS SUSPENSION

Somerset, NJ – November 22, 2004 – MedPointe Pharmaceuticals responded today to recent developments concerning its continued efforts to enforce its intellectual property rights covering its TUSSI-12®D product line.

MedPointe’s TUSSI-12®D brand products are covered by U.S. Patent No. 6,417,206 (“the ‘206 patent”). MedPointe has previously successfully enforced this patent against certain manufacturers to prevent infringement, obtaining consent orders and preliminary injunctions from the U.S. District Court for the District of New Jersey that prevent these parties from offering to sell or selling generic versions of MedPointe’s patented TUSSI- 12®D products.

Although a panel of an appellate court on November 17, 2004 issued an opinion that the preliminary injunction against Hi-Tech Pharmacal Co., Inc., Amityville, NY, should be vacated, MedPointe believes that the preliminary injunction remains in full force and effect, unless and until the appellate court issues a mandate vacating it. Among other things, the preliminary injunction prevents Hi-Tech Pharmacal Co., Inc. from shipping, manufacturing, having manufactured, offering to sell, selling, or importing into the U.S. Tannate 12 D S, a generic version of MedPointe’s TUSSI-12®DS brand suspension product.

On November 19, 2004, Hi-Tech Pharmacal Co., Inc. issued a press release stating that it “plans to begin shipments of its Tannate 12 D S cough and cold product in the near future” but that it “may still be subject to liability based on a claim of patent infringement for sales of Tannate 12 D S.” MedPointe believes that Hi-Tech Pharmacal Co., Inc. remains bound by the preliminary injunction and may not ship, manufacture, have manufactured, offer to sell, sell, or import into the U.S. Tannate 12 D S, unless and until the District Court, acting on a mandate by the appellate court, lifts that injunction.

MedPointe believes that the panel opinion of the appellate court is in error, and agrees with the Chief Judge of the appellate court, who dissented from the panel opinion. MedPointe intends to petition for a rehearing to overturn the opinion and prevent the issuance of any mandate vacating the injunction.

MedPointe notes that even if the preliminary injunction is lifted, the panel of the appellate court stated that its decision “in no way resolves the ultimate question of validity” of MedPointe’s ‘206 patent.

MEDPOINTE PHARMACEUTICALS
MedPointe Pharmaceuticals is a privately held, specialty pharmaceutical company located at 265 Davidson Avenue, Somerset, New Jersey, 08873-4120; 732-564-2200. MedPointe specializes in respiratory, allergy, central nervous system, cough-cold, and pediatric products. The company maintains a manufacturing facility in Decatur, Illinois. For more information on MedPointe, visit www.medpointepharma.com.

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Astelin Ready SprayTM Cited By Institute Of Packaging Professional For Innovative Package Design

Somerset, NJ – November 10, 2004 – The Institute of Packaging Professionals (IoPP) has recognized MedPointe’s ASTELIN Ready-SprayTM with an AmeriStar Award for excellence in consumer product package design in the pharmaceutical/drug category. Ronald Jaketic, Manager of Engineering Projects for MedPointe, accepted the award on behalf of MedPointe at the PACK EXPO International Show 2004 on November 9 in Chicago, Ill.

The award recognizes the innovative new package design for the company’s leading prescription intranasal antihistamine, ASTELIN (azelastine hydrochloride) Nasal Spray, 137 mcg. Introduced in April, the redesigned package offers a new 30 mL bottle featuring a convenient, preassembled spray pump unit and a patented, V-shaped bottom to maximize utilization.

“This new ASTELIN package was designed to provide consumers with a more user-friendly product,” said Paul Edick, President of MedPointe. “We are honored that the IoPP has acknowledged our efforts to enhance patient benefit and increase the product’s ease-of-use.”

The Institute of Packaging Professionals is the leading North American Individual membership organization serving professionals in the packaging community. Each year the organization recognizes industry leaders for innovative and pioneering packaging design at its PACK EXPO International Show.

ABOUT ASTELIN READY-SPRAY, 30 ML

ASTELIN is the fastest-growing antihistamine in new prescriptions since April 2004. ASTELIN Nasal Spray is indicated for the treatment of the symptoms of seasonal allergic rhinitis (in patients five years of age and older) and nonallergic vasomotor rhinitis (in patients 12 years of age and older). According to the Joint Task Force on Practice Parameters in Allergy, Asthma, and Immunology, intranasal antihistamines such as ASTELIN are recommended as first-line treatment for allergic rhinitis. ASTELIN Nasal Spray is well tolerated and relieves a full range of rhinitis symptoms, including tough-to-treat nasal congestion. The most commonly reported adverse events in seasonal allergic rhinitis and nonallergic vasomotor rhinitis patients 12 years of age and older were bitter taste, headache, somnolence, and nasal burning. The adverse event profile in seasonal allergic rhinitis patients five to 11 years of age was similar to that in the adult population.

MEDPOINTE PHARMACEUTICALS
MedPointe Pharmaceuticals is a privately held, specialty pharmaceutical company located at 265 Davidson Avenue, Somerset, New Jersey, 08873-4120; 732-564-2200. MedPointe specializes in respiratory, allergy, central nervous system, cough-cold, and pediatric products. The company maintains a manufacturing facility in Decatur, Illinois. For more information on MedPointe, visit www.medpointepharma.com.

For additional information and/or full prescribing information on ASTELIN® (azelastine hydrochloride) Ready-SprayTM, please call 1-800-598-4856 or visit ASTELIN’s new web site at www.astelin.com.

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articles

MedPointe Announces Sales Force Expansion Signs Agreement with Innovex

Total Wallace Rx Promotional Efforts to Exceed 300 Sales Representatives; Innovex to Provide Sales Force Recruitment and Training

Cranbury, NJ and Parsippany, NJ – January 14, 2002 – MedPointe Inc. and its Wallace Pharmaceuticals Division announced today that they have hired Innovex, a unit of Quintiles Transnational Corp. (NASDAQ: QTRN), to recruit and provide training support for approximately 120 new sales representatives and managers to accelerate sales of several key MedPointe prescription pharmaceutical products. The addition of these 120 individuals to the promotional effort behind MedPointe’s prescription pharmaceutical line will increase MedPointe’s total US promotional field force to approximately 300 persons.

The agreement between MedPointe and Innovex includes the selling effort behind one of MedPointe’s flagship brands, ASTELIN®, its unique nasal spray to treat allergic and non-allergic rhinitis. The Innovex sales managers and representatives will work closely with sales management at MedPointe’s Wallace Pharmaceuticals Division in their commercialization efforts. Under the agreement, Innovex will provide proactive recruiting services based on a wide range of proprietary recruiting resources and methods. Also, as part of this agreement, Innovex will provide consulting services to accelerate Wallace Pharmaceuticals’ sales training programs in order to place qualified sales representatives in the field as quickly as possible.

“This represents an important step forward in our plans to enhance the commercial impact of our portfolio, especially our major respiratory therapeutic, ASTELIN®,” said James S. Burns, MedPointe’s President and Chief Operating Officer. Gary Evans, Vice President-Field Sales, said, “Our product line responds well to direct promotion by our field sales force. The Innovex arrangement allows us to achieve national coverage quickly in order to better support our growing ASTELIN® and RYNA/TUSSI® products.”

Richard Johnson, M.D., Chief Executive Officer, Quintiles Commercialization North America, said: “Providing ‘in-house’ recruiting and training services to build new sales forces can sometimes impose delays on a customer company’s operations. At Innovex, we specialize in rapid deployment of new sales forces to help accelerate customers’ sales. Innovex’s leading capabilities in sales force recruiting puts us at the forefront of this $200 million-dollar industry.”

About MedPointe
MedPointe Inc. is a privately held company located at Half Acre Road, Cranbury, New Jersey, 08512; 609-655-6000. Its prescription pharmaceutical products division, Wallace Pharmaceuticals, specializes in respiratory, pediatric and central nervous system therapies and maintains manufacturing facilities in Cranbury, New Jersey and Decatur, Illinois. Wampole Laboratories, MedPointe’s diagnostics division, distributes a wide range of immunoassay-based diagnostic tests for use by hospitals, physicians and reference laboratories. For more information on MedPointe, Wallace Pharmaceuticals or Wampole Laboratories, visit www.medpointeinc.com.

About Innovex
Innovex, a unit of Quintiles, is the world’s leading commercial solutions provider and offers sales and marketing services designed to accelerate the success of pharmaceutical, biotech and medical device products. Since 1996, Innovex has created more than 94 contract sales forces in the United States, with more than 12,500 representatives who have launched more than 100 established products and 37 new products. For more information, visit www.innovex.com.

Quintiles Transnational Corp. is the world’s leading provider of information, technology and services to bring new medicines to patients faster and improve healthcare. Headquartered near Research Triangle Park, North Carolina, Quintiles Transnational is a member of the S&P; 500 and Fortune 1000. For more information visit the company’s Web site at www.quintiles.com.

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articles

MedPointe Capital Partners To Purchase Carter-Wallace Heathcare Business

Backed by Investment Firms Carlyle and Cypress, Pharmaceutical Executives Set to Build Specialty Healthcare Products Company

Short Hills, NJ – May 8, 2001 – MedPointe Capital Partners, backed by private equity firms The Carlyle Group and The Cypress Group, announced this morning that it has entered into a definitive agreement to purchase the healthcare business of Carter-Wallace, Inc. (NYSE:CAR) in a cash deal valued at approximately $408 million.

In a separate transaction, Carter-Wallace has agreed to sell the assets of its consumer products business for approximately $739 million to Armkel, a partnership of consumer goods company Church & Dwight and the private equity group Kelso & Company. Both transactions must be approved by Carter-Wallace shareholders and receive clearance from various regulatory agencies. CPI Development Corporation, a private holding company that controls approximately 83 percent of the voting power of Carter-Wallace, has entered into an agreement to vote in favor of the transactions, subject to certain limited exceptions. The transactions are expected to be completed in late summer 2001.

In the deal, MedPointe is acquiring Wallace Laboratories, Carter-Wallace’s pharmaceutical arm, and Wampole Laboratories, its diagnostics unit, as well as the rights to the Carter-Wallace name. MedPointe, Carlyle and Cypress, which will collectively invest approximately $275 million in the transaction, were advised in the transaction by Bear, Stearns & Co. Inc., Simpson Thacher & Bartlett and PricewaterhouseCoopers LLP. Bear, Stearns & Co. Inc. has also provided a commitment for up to $225 million of senior bank debt.

“Carter-Wallace is a healthcare products company with a long history and strong assets,” said Anthony H. Wild, Ph.D., MedPointe’s Chairman and CEO. “The job now is to capitalize on those assets through increased emphasis on sales and marketing, product development and licensing. We have a long road ahead of us, but we are confident that the Carter-Wallace healthcare business provides an excellent platform for growth.”

MedPointe’s executives – who have spent most of their careers in the healthcare products industry – will assume senior operating positions at the company once the deal closes. Dr. Wild, who will become Chairman and CEO of the new company, is the former President of the Global Pharmaceutical Sector of Warner-Lambert, where he had worldwide responsibility for the company’s pharmaceutical operations, including research and development. During Dr. Wild’s tenure, he managed sales growth from $2.1 billion to $10 billion, the formation of the Sankyo/Parke-Davis joint venture, the global partnership with Pfizer to market the cholesterol-lowering drug Lipitor®, and the acquisitions of Jouveinal, Agouron, Hickson and gene/Networks.

The other three MedPointe executives will serve as Executive Vice Presidents in the new company, responsible for operations, administration and finance. The senior executive team includes James S. Burns, former Group President at Becton Dickinson and Vice Chairman of HealthCare Ventures; John T.W. Hawkins, former head of the Global Healthcare Sector at executive search firm Russell Reynolds Associates; and Paul S. Herendeen, former Executive Vice President and CFO of Warner Chilcott, a specialty pharmaceutical company recently merged with Galen Holdings, an Irish specialty pharmaceutical company.

MedPointe (www.medpointecapital.com), which is currently headquartered in Short Hills, New Jersey, was founded last year with the intention of building a specialty healthcare products company. “The scale of the large pharmaceutical and diagnostics companies today means that a great deal of emphasis is placed on ‘blockbuster’ products,” explained Dr. Wild. “As a result, there are many excellent mid-level products that don’t receive the support they should. These products may not make strategic sense to a ‘big pharma’ company, but we see a lot of opportunity in them.” After the closing of the sale, MedPointe will be headquartered in the current Carter-Wallace facility in Cranbury, New Jersey.

Dr. Wild and the MedPointe team were attracted to Wallace and Wampole Laboratories because they have a solid foundation of products, including the allergy medicine Astelin®, the muscle relaxant Soma®, the Rynatan/Tussi® cough-cold line and a range of professional laboratory and physician office diagnostic tests. The MedPointe strategy following completion of the deal calls for increased investment in product sales, increased emphasis on new product formulation, and further product acquisitions to accelerate the company’s growth.

The Carlyle Group is a global diversified private equity firm that originates, structures, and acts as an equity investor in management buyouts, corporate partnerships, platform consolidations, private placements and growth investments. Carlyle currently manages approximately $12 billion of capital across twelve institutional funds, including a $3.9 billion domestic leveraged buyout fund. Carlyle has completed approximately 215 transactions, investing over $5.8 billion of equity and purchasing more than $16.4 billion of assets.

The Cypress Group is a private equity investment fund whose objective is to achieve long-term capital appreciation through growth-oriented, privately negotiated equity investments. The Cypress Group currently manages over $3.5 billion of equity capital on behalf of major pension funds, university endowments and other leading financial institutions. To date, The Cypress Group has invested over $1.5 billion in nine transactions. As principals, The Cypress Group has invested a total of approximately $2.3 billion in 21 businesses with an aggregate transaction value of approximately $13.5 billion.

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A New Pharma Company is Born: MedPointe

Backed by Investment Firms Carlyle and Cypress, Pharmaceutical Executives Create MedPointe Inc. and Complete the Acquisition of Carter-Wallace and its Healthcare Business

Cranbury, NJ – October 1, 2001 – A group of healthcare executives, backed by two leading private equity firms, announced today that it has completed the $408-million acquisition of the Healthcare Business and corporate stock of Carter-Wallace, Inc. (formerly NYSE:CAR). Carter-Wallace, Inc. has changed its name to MedPointe Inc.

This acquisition was led by a syndicate of private equity firms headed by The Carlyle Group and The Cypress Group. The syndicate also included Frazier & Company and Ferrer Freeman Thompson & Co. Through this transaction, the investor group acquired Carter-Wallace, Inc. and its two principal Healthcare Businesses, Wallace Pharmaceuticals, a prescription pharmaceutical division, and Wampole Laboratories, its medical diagnostics division.

The acquisition was funded with more than $500 million in equity and debt commitments, including more than $280 million from the equity investors. Bear, Stearns & Co. Inc., which underwrote the initial debt financing commitment, acted as Lead Arranger and Lehman Brothers acted as Co-Arranger for the syndication of $225 million of Senior Secured Credit Facilities in connection with the acquisition. Bear, Stearns & Co. Inc. also advised the equity investors.

“The successful completion of this acquisition concludes nearly a year of hard work by our management team, our investors and our employees and marks the birth of a new company,” said Anthony H. Wild, Ph.D., MedPointe Inc.’s Chairman and CEO. “The healthcare businesses of Carter-Wallace have provided MedPointe with strong operating management, an excellent foundation of products and two highly skilled sales forces. Through this acquisition, we have a wonderful starting point towards fulfilling the promise of MedPointe’s core mission: ‘making medicine better.'” MedPointe plans to pursue a variety of business development initiatives including product acquisitions, line extensions, licensing, co-promotion arrangements and reformulations.

The Wallace Pharmaceuticals product line includes the allergy medicine Astelin®, the only prescription antihistamine approved by the FDA for both seasonal allergic rhinitis and non-allergic (vasomotor) rhinitis. The Wallace line also includes the Rynatan/Tussi® cough-cold line, the muscle relaxant Soma® and the anticonvulsant Felbatol®. The Wampole product line includes a range of professional laboratory and physician office diagnostic products. “We believe that specialty products – marketed and managed effectively – offer substantial opportunities that MedPointe can bring to fruition,” explained Dr. Wild. “Not every product needs to be a ‘blockbuster’ drug in order to be a successful part of the healthcare products market.”

On a pro forma basis, for the twelve months ended March 31, 2001, MedPointe Inc. had consolidated net sales of approximately $220 million. As of October 1, 2001, MedPointe Inc. has approximately 525 full-time employees, including 275 in field sales and sales management.

The management team roster of MedPointe Inc. is comprised of senior, seasoned healthcare executives:

  • Dr. Anthony H. Wild, Chairman and CEO of the new company, is the former President of the Global Pharmaceutical Sector of Warner-Lambert, where he had worldwide responsibility for the company’s pharmaceutical operations, including research and development. During Dr. Wild’s tenure, he managed Warner-Lambert’s pharmaceutical sales growth from $2.1 billion to $10 billion. In addition, he was responsible for the formation of the Sankyo/Parke-Davis joint venture, the global partnership with Pfizer to market the cholesterol-lowering drug Lipitor® and the acquisitions of Jouveinal, Agouron, Hickson and gene/Networks. He is a Founding Partner and CEO of MedPointe Capital Partners, LLC, a private equity capital partnership whose goal was to create a leading company in the specialty pharmaceutical arena.
  • James S. Burns will serve as President and Chief Operating Officer of MedPointe Inc. He was a former Group President at Becton Dickinson, a founding Vice Chairman of HealthCare Ventures and a Partner at Booz Allen & Hamilton. He is a Founding Partner and Managing Director of MedPointe Capital Partners, LLC.
  • John T.W. Hawkins will serve as MedPointe Inc.’s Executive Vice President, Corporate Development and External Affairs. Mr. Hawkins was the former Head of the Global Healthcare Sector at executive search firm Russell Reynolds Associates, and previously, an investment banker at Alex. Brown & Sons. He is also a Founding Partner and Managing Director of MedPointe Capital Partners, LLC.
  • Paul S. Herendeen, Executive Vice President and Chief Financial Officer, brings more than 20 years of experience in the financial services and healthcare industries, most recently as Executive Vice President and Board Member of Galen plc, a public U.K.-based pharmaceutical company.
  • Bernardo L. Tafur will serve as MedPointe Inc.’s Executive Vice President, Human Resources and Administration. He was formerly the Senior Vice President, Human Resources of Pfizer Inc.’s Pharmaceuticals Group.
  • Beth P. Hecht, Senior Vice President, General Counsel and Secretary, has more than 14 years of corporate legal experience, having worked as Vice President, General Counsel and Secretary for Warner Chilcott plc, Alpharma Inc. and ChiRex, Inc.
  • Thomas G. Gerstmyer will continue as President of Wallace Pharmaceuticals, the flagship pharmaceutical division of MedPointe Inc.
  • John Bridgen, Ph.D., will continue as President of Wampole Laboratories, MedPointe Inc.’s medical diagnostics division.
  • Gerald L. Messerschmidt, M.D., FACP, will serve as MedPointe Inc.’s Senior Vice President, Medical and Scientific Affairs. Prior to joining MedPointe Inc., he held senior executive positions at C.R. Bard, Inc., DNX Corporation and Ciba-Geigy Corporation.
  • Bruce C. Friedman will serve as Corporate Vice President, Supply Chain Management. He previously served as Carter-Wallace Inc.’s Vice President, Operations for the Manufacturing Division.
  • Timothy G. Henner will serve as Vice President and Corporate Controller of MedPointe Inc. Previously, he served as Carter-Wallace, Inc.’s Vice President and Controller, Manufacturing and Quality Control.
  • Michael A. Tropiano will serve as Vice President and Corporate Treasurer of MedPointe Inc. He served previously as Carter-Wallace, Inc.’s Assistant Treasurer.

MedPointe Inc. has gathered a group of distinguished senior executives to constitute its Board of Directors. Dr. Wild will serve as Chairman of the newly formed board. MedPointe Inc. Board Members will also include Richard U. DeSchutter, retired Chairman and CEO of GD Searle and former Chairman & CEO of DuPont Pharmaceuticals; Ernest J. Larini, former Executive Vice President and Chief Financial Officer of Warner-Lambert Company; W. Robert Dahl, a Managing Director and Head of Healthcare investing at The Carlyle Group; Kenneth S. Abramowitz, a Managing Director at The Carlyle Group and former healthcare analyst at Sanford C. Bernstein & Co. where he covered the medical-supply, hospital-management and HMO industries; and William L. Spiegel, a Managing Director at The Cypress Group who leads the firm’s efforts in the healthcare and financial services sectors. Later this month, it is anticipated that The Cypress Group will nominate another Director for appointment to the Board.

MedPointe Inc. is a privately held company located at Half Acre Road, Cranbury, New Jersey, 08512; 609-655-6000. MedPointe expects to relocate to new corporate offices in Bridgewater, New Jersey in the second quarter of 2002. Its prescription pharmaceutical products division, Wallace Pharmaceuticals, specializes in respiratory, pediatric and central nervous system therapies and maintains manufacturing facilities in Cranbury, New Jersey and Decatur, Illinois. Wampole Laboratories, MedPointe’s diagnostics division, distributes a wide range of immunoassay-based diagnostic tests for use by hospitals, physicians and reference laboratories. For more information on MedPointe, Wallace Pharmaceuticals or Wampole Laboratories, visit www.medpointeinc.com.

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ASTELIN® (AZELASTINE HYDROCHLORIDE) NASAL SPRAY EFFECTIVE IN PATIENTS WHOSE ALLERGY SYMPTOMS RESPONDED INADEQUATELY TO TREATMENT WITH ALLEGRA®

Clinical Data Published in Leading Medical Journal as Fall Allergy Season Begins

Somerset, NJ – August 16, 2004 – ASTELIN® Nasal Spray provided effective symptom relief for patients with moderate-to-severe seasonal allergic rhinitis who had an unsatisfactory response to treatment with Allegra® (fexofenadine hydrochloride), according to a clinical study published in the August issue of Annals of Allergy, Asthma & Immunology.

“Our findings show that ASTELIN is an effective treatment option for patients with seasonal allergic rhinitis who do not respond well to fexofenadine,” reported Craig LaForce, MD, study investigator and Medical Director, North Carolina Clinical Research. “In fact, ASTELIN is an excellent alternative for patients who find themselves using multiple oral antihistamines or frequently switching antihistamines to find satisfactory relief.”

A similar study, published in the August 2003 issue of Annals of Allergy, Asthma & Immunology, showed ASTELIN to be an effective option for patients who had experienced unsatisfactory relief of moderate-to-severe allergic rhinitis symptoms with Claritin® (loratadine).

“Given the growing body of clinical data that reinforces the efficacy of azelastine nasal spray in treating allergic rhinitis, ASTELIN should be considered an excellent option for first-line treatment,” commented Dr. LaForce.

Mid-August marks the beginning of the ragweed (fall allergy) season in much of the United States, according to the American Academy of Allergy, Asthma and Immunology.

THE STUDY
This was a multicenter, placebo-controlled, double-blind trial of 335 patients who had experienced unsatisfactory results with a seven-day course of fexofenadine monotherapy. Patients who had an inadequate response to fexofenadine were divided into three treatment groups: 1) ASTELIN Nasal spray and oral placebo; 2) ASTELIN Nasal Spray and fexofenadine; or 3) placebo nasal spray and oral placebo for a two-week treatment period. The TNSS – defined as the sum of individual symptom severity scores for runny nose, sneezing, itchy nose, and nasal congestion – determined drug efficacy.

After two weeks of treatment, the mean improvement from baseline in TNSS with ASTELIN Nasal Spray was significantly greater than with placebo. Further, the combination of ASTELIN and fexofenadine showed no additional clinical benefit compared to ASTELIN monotherapy.

ALLERGIC RHINITIS
Allergic rhinitis is the fifth most prevalent chronic disease in the United States, affecting up to 40 million adults and children each year. Allergic rhinitis costs the nation approximately $5.3 billion in direct and indirect costs (including time lost from work and school) and accounts for about 10,000 absences on a typical school day. It also can lead to complications, including sinusitis, Eustachian-tube dysfunction, ear infections, asthma, and sleep disturbances.

Current prescription and over-the-counter treatments include oral and intranasal antihistamines, oral and intranasal decongestants, intranasal corticosteroids, mast-cell stabilizers, and leukotriene- receptor antagonists. If the physician determines that allergen avoidance and pharmacotherapy do not provide sufficient relief, and if symptoms are sufficiently severe, he/she may suggest desensitization (immunotherapy).

ASTELIN® (AZELASTINE HYDROCHLORIDE) NASAL SPRAY, 137 MCG
ASTELIN Nasal Spray is indicated for the treatment of the symptoms of seasonal allergic rhinitis (patients five years of age and older) and nonallergic vasomotor rhinitis (patients 12 years of age and older). According to the Joint Task Force on Practice Parameters in Allergy, Asthma, and Immunology, an intranasal antihistamine, such as ASTELIN, is recommended as first-line treatment for allergic rhinitis. ASTELIN is the only antihistamine approved for rhinitis patients with nasal congestion.

The most commonly reported adverse events in seasonal allergic rhinitis and nonallergic vasomotor rhinitis patients 12 years of age and older were bitter taste, headache, somnolence, and nasal burning. The adverse event profile in seasonal allergic rhinitis patients five to 11 years of age was similar to that in the adult population. Discontinuation rates due to adverse events in patients taking ASTELIN in the seasonal allergic rhinitis and nonallergic vasomotor rhinitis clinical trials were no different than those for placebo.

Please see full Prescribing Information, available at www.astelin.com.

MEDPOINTE PHARMACEUTICALS
MedPointe Pharmaceuticals is a privately held, specialty pharmaceutical company with headquarters at 265 Davidson Avenue, Somerset, New Jersey, 08873-4120; 732-564-2200. MedPointe, which specializes in allergy, respiratory, central nervous system, cough-cold, and pediatric products, has a manufacturing facility in Decatur, Illinois. For more information about the company, please visit www.medpointepharma.com.

For additional information and/or full Prescribing Information on ASTELIN Nasal Spray, please call 1-800-598-4856 or visit www.astelin.com.

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MedPointe’s Expanded Sales Force Will Promote OPTIVAR® To Eye-Care Physicians

Somerset, NJ and Rochester, NY – December 7, 2004 – MedPointe Pharmaceuticals announced today that its expanded sales force will now have sole responsibility for promoting MedPointe’s OPTIVAR® (azelastine hydrochloride ophthalmic solution 0.05%) to the ophthalmic/eye-care community starting January 1, 2005. Bausch & Lomb, a global leader in eye health, had provided sales support for OPTIVAR after MedPointe acquired the medication in the second quarter of 2003. Since then, MedPointe has doubled its overall sales force in Primary Care and, most recently, expanded its Allergy Specialty sales force by 33 percent.

OPTIVAR is a sterile ophthalmic solution indicated for the treatment of itching of the eye associated with allergic conjunctivitis.

“While Bausch & Lomb has provided MedPointe with support in promoting OPTIVAR to eye-care specialists, we now have the resources and the capability to cover this important physician segment with the recent expansions of our Specialty Allergy and Primary Care field forces,” said Paul Edick, president of MedPointe. “We are committed to calling on selected ophthalmologists who treat allergic conjunctivitis patients, as well as the allergy, primary care, and ear, nose and throat specialists whom we normally see. The expansion of our allergy sales force to cover more eye-care physicians reaffirms our belief that OPTIVAR has great market potential, given its ability to target both the early- and late-phase allergic response in the eye.”

Paul G. Howes, Bausch & Lomb senior vice president and president of the Americas Region, said, “With the anticipated approval of new products in our own portfolio and a strategic review of our marketing priorities, Bausch & Lomb will focus on our own products. We wish MedPointe continued success with OPTIVAR.”

ABOUT OPTIVAR
OPTIVAR (azelastine hydrochloride ophthalmic solution, 0.05%) is a sterile ophthalmic solution indicated for the treatment of itching of the eye associated with allergic conjunctivitis in patients as young as 3 years of age. In controlled, multidose studies, the most frequently reported adverse events were transient eye burning/stinging, headache, and bitter taste. Discontinuation due to these adverse events was less than 1 percent. OPTIVAR is contraindicated in persons with known hypersensitivity to any of its components.

MEDPOINTE PHARMACEUTICALS
MedPointe Pharmaceuticals is a privately held, specialty pharmaceutical company located at 265 Davidson Avenue, Somerset, New Jersey, 08873-4120; 732-564-2200. MedPointe specializes in respiratory, allergy, central nervous system, cough-cold, and pediatric products. The company maintains a manufacturing facility in Decatur, Illinois. For more information on MedPointe, visit www.medpointepharma.com

For additional information and/or full Prescribing Information for OPTIVAR®, please call 1-800-598-4856.

BAUSCH & LOMB
Bausch & Lomb is the eye health company, dedicated to perfecting vision and enhancing life for consumers around the world. Its core businesses include soft and rigid gas permeable contact lenses and lens care products, and ophthalmic surgical, and pharmaceutical products. The Bausch & Lomb name is one of the best known and most respected healthcare brands in the world. Celebrating its 150th anniversary, the Company is headquartered in Rochester, New York. Bausch & Lomb’s 2003 revenues were $2 billion; it employs approximately 11,500 people worldwide and its products are available in more than 100 countries. More information about the Company can be found on the Bausch & Lomb Web site at www.bausch.com. Copyright Bausch & Lomb.

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MEDPOINTE ACQUIRES OPTIVAR®, FAST-GROWING RX TREATMENT FOR ITCHY EYES IN ALLERGIC CONJUNCTIVITIS

Purchase Strengthens MedPointe’s Allergy Franchise, Leverages Its Sales Force

Somerset, NJ – April 29, 2003 – MedPointe Inc. announced that it has completed the acquisition of all U.S. and Canadian rights to Optivar® (azelastine hydrochloride), a prescription-only treatment for itching of the eye associated with allergic conjunctivitis in adults and children ages three and older. Comprised of the same active ingredient, Optiva® is complementary to MedPointe’s flagship product, Astelin®, and a significant addition to the Company’s growing allergy/respiratory franchise.

Optivar® will be detailed in a co-primary position with Astelin® by MedPointe’s 304-territory U.S. sales force and promoted to more than 50,000 primary care physicians, allergists and ear, nose and throat specialists. In connection with the acquisition, MedPointe assumed a co-promotion agreement with Bausch & Lomb, which will continue to co-promote the product to the ophthalmic/eye care community. Launched in 2000 with exclusivity until 2010, Optivar® generated net sales in 2002 of $13 million and is experiencing year-over-year annual prescription growth in excess of 30 percent.

“We are extremely pleased to announce this strategically important acquisition for MedPointe,” said Anthony H. Wild, Ph.D., MedPointe’s Chairman and Chief Executive Officer. “Optivar is a young product with strong growth prospects that extends our presence in the allergy category and provides our sales force with another high-growth niche product to promote just as the allergy season is upon us. We have pursued this acquisition for a number of months, and its successful completion reaffirms our commitment to building a substantial specialty pharmaceuticals company.”

Allergic conjunctivitis is the most common ocular allergy, affecting 25 percent of the general population and 60 percent of people with nasal allergies, according to the American Academy of Allergy, Asthma and Immunology (AAAAI). The symptoms of allergic conjunctivitis – itching, burning and redness of the eyes – are highly seasonal and are triggered by the action of histamines in response to airborne allergens such as pollen, mold and dust. While sufferers would benefit from a prescribed treatment, few seek a physician’s care and most self-medicate with over-the-counter drugs. The US market for ocular allergy treatments is estimated at approximately $280 million.

Under the terms of the sale, MedPointe acquired Optivar®, including all commercial and intellectual property rights in the United States and Canada, from Viatris, Inc., Viatris GmbH & Co. KG, and Muro Pharmaceuticals, Inc. The purchase price was not disclosed.

MedPointe Inc. is a privately held specialty pharmaceutical company located at 265 Davidson Avenue, Suite 300, Somerset, New Jersey, 08873-4120; 732-564-2200. MedPointe specializes in respiratory, allergy, central nervous system, cough/cold and pediatric products. The company maintains a manufacturing facility in Decatur, Ill. For more information on MedPointe, visit www.medpointepharma.com.

For further information, contact:

John Hawkins
Executive Vice President
MedPointe, Inc.
732-564-2233
[email protected]
www.medpointepharma.com