U.S. Food and Drug Administration (FDA)
The U.S. Food and Drug Administration (FDA) permits violet 2 to be used for coloring externally applied cosmetics and personal care products, and externally applied drugs when violet 2 conforms to FDA specifications. Externally applied products do not include products intended for use on the lips, or products intended for use in the eye area. According to U.S. regulations, all violet 2 manufactured for use in products is subject to certification by the FDA. This certification process ensures that the strict chemical and identity specifications set by FDA are met.
Expert Panel for Cosmetic Ingredient Safety
The Expert Panel for Cosmetic Ingredient Safety has deferred evaluation of this ingredient because the safety has been assessed by FDA. This deferral of review is according to the provisions of the Expert Panel procedures.
All color additives used in foods, drugs and cosmetics in the United States must be approved by FDA and listed in the Code of Federal Regulations. In some cases, FDA requires that each batch of color produced for use in regulated products can be used only if it is certified by the agency to meet strict specifications. FDA maintains a laboratory especially for this purpose and color manufacturers must pay a fee to support this activity. FDA only approves colors after extensive review of all safety data and publication of the basis for its approval in the Federal Register.
You can find out more about FDA regulation of colors at: http://www.cfsan.fda.gov/~dms/cos-col.html
Link to FDA Code of Federal Regulations for violet 2
Violet 2 is listed as CI 60725 in the Cosmetics Directive of the European Union (see Annex IV) and may be used in all cosmetics and personal care products. When used in cosmetic products in the European Union, this ingredient must be called CI 60725.
Link to the EU Cosmetic Regulation:
You can learn more about the regulation and labeling of colors at: