Antonio Mcgowan
Ed Hardy cologne is regulated as a cosmetic by the FDA. The FDA does not require cosmetic products and ingredients, other than colour additives, to have approval before they go on the market. However, the FDA can take action against cosmetics on the market that are in violation of the law.
| Characteristics | Values |
|---|---|
| Introduced in | 2008 |
| Fragrance notes | Amber, bergamot, mandarin, clary sage, thuja, sequoia |
| Use | Casual |
What You'll Learn
Ed Hardy cologne is for men and was launched in 2008
Ed Hardy cologne for men was launched in 2008 from designer Christian Audigier. Known for his tattoo artwork, Ed Hardy brings these intricate images to each Ed Hardy men cologne bottle and packaging.
The cologne is a woody aromatic fragrance with top notes of mandarin orange, bergamot, and clary sage; a middle note of mint; and base notes of amber and musk.
Ed Hardy cologne has a variety of scents, including Love & Luck, Hearts & Daggers, Villain, Love is True Til Death, and Born Wild.
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The cologne has top notes of mandarin, bergamot, and clary sage
The Ed Hardy cologne for men, launched in 2008, has top notes of mandarin, bergamot, and clary sage. The cologne is described as woody and aromatic, with a fresh, spicy opening. The top notes of mandarin, bergamot, and clary sage are complemented by middle notes of mint and base notes of amber and musk. The cologne is marketed towards younger men, with its intricate tattoo-inspired bottle design and packaging. The Ed Hardy cologne is a safe, simple, and affordable option for those looking for an everyday fragrance.
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The Ed Hardy cologne bottle features intricate tattoo artwork
The cologne bottle's design is a collaboration between Hardy and Christian Audigier, who licensed Hardy's artwork for a clothing line in the early 2000s. Audigier, a renowned designer from Avignon, France, became well-known for his work with Hardy, and the Ed Hardy brand became associated with celebrities.
The Ed Hardy cologne bottle's intricate tattoo artwork is a reflection of Hardy's unique style, which blends Japanese tattoo aesthetics and techniques with American styles of work. The bottle's design is an example of Hardy's fine art mentality, which helped elevate tattoos from a subculture to pop culture.
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The cologne is regulated as a cosmetic by the FDA
The U.S. Food and Drug Administration (FDA) regulates cosmetics under the Federal Food, Drug, and Cosmetic Act (FD&C Act) and the Fair Packaging and Labeling Act (FPLA). The FD&C Act defines cosmetics by their intended use, as "articles intended to be rubbed, poured, sprinkled, or sprayed on, introduced into, or otherwise applied to the human body...for cleansing, beautifying, promoting attractiveness, or altering the appearance."
The cologne is intended to be applied to the body to make the person more attractive, so it is a cosmetic under the law and is regulated by the FDA.
The law does not require FDA approval before cosmetics go on the market, but there are laws and regulations that apply to cosmetics on the market in interstate commerce. The FDA can take action against cosmetics on the market that are in violation of these laws, as well as companies and individuals who market such products.
The FDA also requires a list of ingredients for cosmetics marketed on a retail basis to consumers. However, under U.S. regulations, fragrance and flavor ingredients can be listed simply as "Fragrance" or "Flavor."
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The cologne is not FDA-approved
The U.S. Food and Drug Administration (FDA) does not require cosmetic products and ingredients, except for colour additives, to have FDA approval before they go on the market. However, the FDA can take action against products on the market that are in violation of the law, as well as companies and individuals who market such products.
The FDA's legal authority over cosmetics is different from its authority over other products it regulates, such as drugs, biologics, and medical devices. Under the law, cosmetic products and ingredients do not need FDA premarket approval. However, the FDA can pursue enforcement action against products on the market that are not in compliance with the law, or against firms or individuals who violate the law.
The FDA has consistently advised manufacturers to use whatever testing is necessary to ensure the safety of their products and ingredients. The FDA has stated that:
> The safety of a product can be adequately substantiated through (a) reliance on already available toxicological test data on individual ingredients and on product formulations that are similar in composition to the particular cosmetic, and (b) performance of any additional toxicological and other tests that are appropriate in light of such existing data and information.
The FDA does not function as a private testing laboratory and does not recommend private laboratories to consumers or manufacturers for sample analysis.
The two most important laws pertaining to cosmetics marketed in the United States are the Federal Food, Drug, and Cosmetic Act (FD&C Act) and the Fair Packaging and Labeling Act (FPLA). The FDA regulates cosmetics under the authority of these laws.
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Frequently asked questions
The FDA does not approve cosmetics before they go on the market. However, the FDA can take regulatory action if they have reliable information that a cosmetic is adulterated or misbranded.
The FDA may take action through the Department of Justice in the federal court system to remove adulterated and misbranded cosmetics from the market. The FDA can also request a federal district court to issue a restraining order against the manufacturer or distributor of the violative cosmetic.
The FDA considers a cosmetic to be adulterated if it bears or contains any poisonous or deleterious substance which may render it injurious to users under the conditions of use prescribed in the labeling thereof, or under conditions of use as are customary and usual. The FDA considers a cosmetic to be misbranded if its labeling is false or misleading in any particular.
Yes, the FDA can and does inspect cosmetic manufacturing facilities to ensure cosmetic product safety and determine whether cosmetics are adulterated or misbranded under the FD&C Act or FPLA.
The FDA does not function as a private testing laboratory, but it does collect samples for examination and analysis as part of cosmetic facility inspections, import inspections, and follow-up to complaints of adverse events associated with their use.
