The Pharma Data

JUNE 18, 2021

June 8, 2021 /PRNewswire/ — Allergan Aesthetics, an AbbVie company (NYSE: ABBV ), is changing the way BOTOX ® Cosmetic, the #1 selling neurotoxin treatment 1 , is connecting with consumers. “BOTOX ® Cosmetic is honoring and celebrating the dynamic people who use our products. . IRVINE, Calif.

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Cloudbyz

MAY 26, 2023

The cosmetics and personal care industry is one where customer trust is paramount, given that the products are applied directly to the skin, hair, and body. By doing so, these solutions help protect consumers and maintain the integrity of the brand. Integration with Other Systems Safety vigilance solutions are not standalone systems.

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BioTech 365

NOVEMBER 30, 2020

Lygos and High Beauty Sign Agreement to Co-Develop and Commercialize Cosmetic Products Containing Rare Cannabinoids Lygos and High Beauty Sign Agreement to Co-Develop and Commercialize Cosmetic Products Containing Rare Cannabinoids Co-branded High & Bye Refining Oil and Clearing Gel to … Continue reading →

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XTalks

NOVEMBER 14, 2022

In the US, it’s against the law to use the carcinogenic color additive Red 3 in cosmetics, such as lipsticks or blush or topicals. As a result, in 1990, the agency eliminated certain “provisionally listed” uses of the chemical — meaning cosmetics and externally applied drugs. But those steps were never taken.

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XTalks

JANUARY 10, 2022

This entails abstaining from animal products including food, clothing and cosmetics. This year, several high-profile companies, along with smaller brands, are launching new items and campaigns for Veganuary 2022. On the sweet side, ice cream brand Magnum launched mini versions of its vegan flavors : Vegan Classic and Vegan Almond.

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FDA Law Blog

MARCH 6, 2024

The American Conference Institute (“ACI”) will be hosting a series of go-to forums on critical topics including novel therapeutics, cosmetics/personal care products and Paragraph IV disputes. Claud will be featured at the Legal, Regulatory, and Compliance Forum on Cosmetics & Personal Care Products in New York, NY.

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XTalks

JANUARY 19, 2021

This includes some flavored e-cigarettes imported to the US that do not meet Federal Food, Drug and Cosmetic Act (FD&C Act) requirements, as amended by the Family Smoking Prevention and Tobacco Control Act (Tobacco Control Act).

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Fossil Remedies

APRIL 7, 2020

150+ Skin & Cosmetic Products. It has a significant presence in brands across all therapeutic segment like from cough & cold to life threatening serious diseases. They offer pharma franchise to interested parties. Some of their product ranges are: 400+ Antibiotics and general products. 150+ Cardiac & Diabetes Product.

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XTalks

FEBRUARY 16, 2023

In a TV ad called “ Taye Diggs Takes on His Insomnia ,” the actor best known for his role in the Grey’s Anatomy spinoff Private Practice shares his own sleep troubles and how insomnia impacts his days and nights, in a nod to the brands original Seize the Night and Day commercial. billion during the same period.

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Roots Analysis

JULY 28, 2024

While cosmetic procedures can effectively target specific aging concerns like deep wrinkles, sagging skin, and volume loss, they may not comprehensively improve the overall skin quality. One example of a successful clean beauty brand is Tata Harper, which offers a range of skincare products made with 100% natural and non-toxic ingredients.

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XTalks

SEPTEMBER 4, 2020

Nowadays, the word’s meaning is commonly extended to refer to non-food products—such as clothing, cosmetics, and medicine—that are made without animal-derived substances. The word vegan was initially defined as a diet free of animal-based foods (such as meat, dairy products, eggs and honey.)

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XTalks

APRIL 14, 2021

The US Food and Drug Administration (FDA) defines color additives as “any substance that imparts color to a food, drug, cosmetic, or the human body. In Europe, brands like Nestlé use radish, lemon and red cabbage extracts as a food coloring in their chocolates. 40 and yellow food dyes no.

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FDA Law Blog

DECEMBER 21, 2023

Those who attended their annual Enforcement, Litigation, and Compliance Conference holiday reception earlier this month got a sneak peek at this new branding effort with the unveiling of the association’s new logo ( here ). The new logo — and a host of other new association branding—will be rolling out throughout 2024.

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XTalks

APRIL 26, 2021

The marker may soon be found on food and beverage products, pet food, dietary supplements, cosmetics and more. In terms of the certification marker, the UFA hired branding agency Modern Species to design the marker for food packaging. Even before the term was formally defined, upcycled foods had been gaining momentum.

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XTalks

NOVEMBER 24, 2022

According to the warning letters, these products are considered adulterated under “section 402(a)(2)(C)(i) of the Federal Food, Drug, and Cosmetic Act (the FD&C Act), 21 U.S.C. Other major brands like PepsiCo and Carl’s Jr. 342(a)(2)(C)(i), because they bear or contain an unsafe food additive. 331(ll) and 331(a).”.

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XTalks

FEBRUARY 8, 2021

Like generic forms of synthetic pharmaceuticals, biosimilars have the advantage of being less costly compared to their branded counterparts. Some prescribers and pharmacists have been hesitant to give patients biosimilar forms of biologic drugs over concerns that they may not be as safe or effective as the branded product.

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XTalks

MARCH 13, 2024

This led people to seek it off-label for cosmetic weight loss, a phenomenon many say is partly to blame for the current shortages of both Novo and Lilly’s GLP-1 drugs. Novo’s weight loss version of Ozempic is branded Wegovy (semaglutide). This isn’t the first time the GLP-1 drugs made it to the Oscars.

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Pharma Marketing Network

APRIL 4, 2022

Many of the medical device and pharma companies are aware of this, and the professional side of AAD.org has benefitted from this relationship, but I noticed during the show that many of the cosmetic and hygiene brands were completely unaware that they could be advertising on the patient side of the website.

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Fossil Remedies

JUNE 18, 2020

A PCD pharma company which gives products, support and brand name to its franchise partner is also called the “PCD pharma franchise company” or “pharma franchiser”. It has a significant presence in brands across all therapeutic segment like from cough & cold to life threatening serious diseases. 150+ Skin & Cosmetic Products.

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XTalks

OCTOBER 10, 2024

The compounding industry argues that many patients are still facing challenges in obtaining the medications, despite the FDA’s assessment, and that compounded versions offer an essential alternative for those unable to access the branded drugs. The removal of GLP-1 receptor agonists from the list has significant implications.

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Roots Analysis

JANUARY 17, 2024

However, the spotlight now shifts to tirzepatide, a drug developed by Lilly and approved in 2022 under the brand name Mounjaro for treating type 2 diabetes. As the drug gains momentum, the demarcation between medical and cosmetic applications becomes increasingly nuanced.

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XTalks

JULY 1, 2024

BBB Foods offers a variety of products, including household cleaning supplies, personal hygiene items, cosmetics, beauty products, pharmaceuticals and general merchandise. The company provides a mix of branded, private label and spot products, catering primarily to low-to-middle income households through online channels.

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The Pharma Data

FEBRUARY 5, 2021

” said Dr. Sabrina Fabi , Board Certified Dermatologist and Associate Research Director at Cosmetic Laser Surgery in San Diego. American Society for Dermatologic Surgery (ASDS) consumer survey on cosmetic dermatologic procedures 2018 available at [link]. For more information and to find a provider near you, visit [link].

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Pharmacy Checkers

NOVEMBER 21, 2019

Wikipedia has an extremely long page aptly called Criticism of the Food and Drug Administration , much of it having to do with its role with prescription drugs, and less so other sectors, such as food, tobacco and cosmetics. . and other high-income countries.

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The Pharma Data

MARCH 15, 2022

To further facilitate generic drug development, and to assist the generic pharmaceutical industry in this process, the FDA publishes product-specific guidances (PSGs) describing the agency’s current thinking and expectations on how to develop generic drug products that are therapeutically equivalent to their brand name counterparts.

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The Pharma Data

NOVEMBER 10, 2020

coli O157:H7 strain found by Michigan Department of Agriculture and Rural Development (MDARD) in Tanimura & Antle brand packaged single head romaine lettuce. brand packaged single head romaine lettuce with a pack date of Oct. SILVER SPRING, Md. , coli O157:H7 illnesses that matches the E. SOURCE U.S.

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pharmaphorum

FEBRUARY 12, 2021

Though most people will know of these toxins through Allergan’s ‘Botox’ brand name and its association with cosmetic surgery, they can be used for a wide variety of medical indications and are often used to relieve spasticity in patients following stroke, traumatic brain injury or other neurological conditions.

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The Pharma Data

MAY 18, 2021

GSK Consumer Healthcare (GSKCH), the world-leading consumer healthcare business, announced today that it is partnering with two global packaging suppliers to launch fully recyclable toothpaste tubes across its specialist and science-based oral health brands, including Sensodyne, parodontax and Aquafresh. About GSK Consumer Healthcare.

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XTalks

SEPTEMBER 28, 2023

Parabens, which are also prevalent in cosmetics, can interfere with the regular operation of human hormonal systems, affecting both male and female reproductive health, development, fertility and birth results. The substance, created by binding vegetable oil with bromine, adds density to the flavor mixture.

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XTalks

NOVEMBER 7, 2023

Some may even extend their expertise to consumer goods sectors, including cosmetic brands. Their expertise is often sought by organizations ranging from medical device manufacturers and biotech companies to pharmaceutical corporations.

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FDA Law Blog

AUGUST 11, 2024

Presenting only information about the benefits or efficacy of a prescription drug, like AUVI-Q, without any risk information is considered a false or misleading presentation under the Federal Food, Drug and Cosmetic Act (FDCA), and is considered misbranding of the product. August 2024 Untitled Letter to Mirati Therapeutics Inc.

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The Pharma Data

MAY 27, 2022

On Tuesday, the FDA announced that it informed Kendal Nutricare that the agency is exercising enforcement discretion for the importation of certain infant formula under the Kendamil brand. store shelves beginning in June. Source link: [link].

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The Pharma Data

NOVEMBER 26, 2020

We have also launched several new product offerings, most notably a dark chocolate coin (each infused with 20mg CBD) and some skin care/cosmetics selections. The record results achieved on November 25, 2020 were followed up by another very strong showing on Thanksgiving Day (November 26, 2020).

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Intouch Solutions

JUNE 30, 2022

47% of those had made in-game purchases, and 37% had purchased virtual cosmetic items. But brands are increasingly going to have to address this unfamiliarity, and normalize therapeutics that aren’t just made out of cellulose and proteins. And 79% of their 3,000 survey respondents said that they had already – not someday!

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FDA Law Blog

SEPTEMBER 15, 2022

Without further discussion or explanation, FDA asserts that the requirement for the placement of the statement of identity “in direct conjunction” with the brand or proprietary name “ implies that the proprietary name and the statement of identity should not be separated by any intervening matter.” underline added).

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FDA Law Blog

APRIL 30, 2021

According to the press release on the bill: The Simplifying the Generic Drug Application Process Act repeals section 505(j)(2)(C) of the Food Drug and Cosmetic Act (FDCA) so that sponsors can submit generic drug applications (ANDAs) without the need for the U.S. Food and Drug Administration (FDA) to first grant a suitability petition.

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FDA Law Blog

APRIL 30, 2021

According to the press release on the bill: The Simplifying the Generic Drug Application Process Act repeals section 505(j)(2)(C) of the Food Drug and Cosmetic Act (FDCA) so that sponsors can submit generic drug applications (ANDAs) without the need for the U.S. Food and Drug Administration (FDA) to first grant a suitability petition.

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