- Alpha & Beta Hydroxy Acids
- Anti-Acne Agents
- Anti-Aging Agents
- Anti-Dark Circles Agents
- Anti-Wrinkle Agents
- Antioxidants
- Antiperspirants
- Bases, Prefabricated
- Botanical Extracts
- Bulk Ingredients
- Catalog & Books
- Colors & Color Blends
- Complete Kits
- Conditioners
- Containers & Bags
- Emollients
- Emulsifiers
- Equipment
- Exfoliants
- Hair Repair Agents
- Humectants
- Instant Cold Emulsifiers
- Liposomes
- Natural Butters
- Natural Oils
- Natural Powders
- Natural Waxes
- Nourishing Agents
- Oily Skin Regulators
- Pearlizers
- Perfume Ingredients
- Polymers
- Preservatives
- Proteins
- Regenerating & Soothing Agents
- Self-Tanners
- Silicones
- Skin-Lightening Agents
- Solvents & Stabilizers
- Sunscreens
- Surfactants
- Texturizers & Powders
- Thickeners
- Vitamins
Labeling of Cosmetics
| Proper labeling is an important aspect of marketing a cosmetic or personal care product. Labeling is used to help inform consumers of a product's intended use and any related warnings, its ingredients and net quantity of contents, and its place of manufacture or distribution. The FDA regulates cosmetic labeling under the authority of both the Food, Drug, and Cosmetic Act (FD&C Act) and the Fair Packaging and Labeling Act (FPLA). These laws and their related regulations are intended to protect consumers from health hazards and deceptive practices and to help consumers make informed decisions about the personal care products they purchase. As part of the prohibition against false or misleading information, no cosmetic may be labeled or advertised with statements suggesting that the FDA has approved the product. This applies even if the manufacturing establishment is registered or the product is on file with FDA's Voluntary Cosmetic Registration Program. All labeling information that is required by US law or regulation must be in English. The only exception to this rule is for products distributed solely in a US territory where a different language is predominant, such as Puerto Rico. |
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| Principal Display Panel (PDP) | ||||||||||||||||||||||||||||||||||||||||
| The Principal Display Panel (PDP) of the label is the part of the label most likely displayed or examined under customary conditions of display for sale. It is on the outer container which usually is a box, folding carton, wrapper etc. holding the inner (immediate) container. If there is no outer container then the PDP is placed on the immediate container holding the cosmetic product. The area of the PDP is for a rectangular package one entire side, for a cylindrical package 40% of height x circumference, and for any other shape of container 40% of total container surface, excluding top, bottom, neck, shoulder, and flanges. There are specific requirements for the form of stating the required information including panel display, panel size, style and size of letters, background contrast, and obscuring designs. For more details please check the FDA/CFSAN Cosmetics Labeling Manual. |
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| Information Panel (IP) | ||||||||||||||||||||||||||||||||||||||||
| The Information Panel (IP) of the label refers to a panel other than the PDP that can accommodate label information where the consumer is likely to see it. | ||||||||||||||||||||||||||||||||||||||||
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More Information |
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| For more detailed information including labeling of product assortments, branded shade lines, trade-secret ingredients, direct mail cosmetics, and off-package ingredient labeling please check the FDA's website or download the FDA/CFSAN Cosmetics Labeling Manual. | ||||||||||||||||||||||||||||||||||||||||


