Cosmetic Defined in FD&C Act, Section 201 (i) Articles intended for: Cleansing Beautifying Promoting attractiveness Altering the appearance Excludes S

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Cosmetics and Color Additives Personal Care Product Council GMP Workshop November 10, 2010 Presented by Richard Chiang Compliance Manager FDA Los Angeles Import Operations Cosmetics Scope Used by most Americans every day Examples: Moisturizers, other skin preparations Hair care, hair dyes, hair straighteners Makeup, nail polishes Shaving preparations Perfumes Toothpastes, mouthwashes Face and body cleansers, deodorants Over 8 billion personal care products sold in U.S. annually Over $60 billion in annual sales 1

Cosmetic Defined in FD&C Act, Section 201 (i) Articles intended for: Cleansing Beautifying Promoting attractiveness Altering the appearance Excludes Soap Drug Defined in FD&C Act, Section 201 (g) Articles intended-- for use in the diagnosis, cure, mitigation, treatment, or prevention of disease to affect the structure or any function of the body of man or other animals 2

Cosmetic vs. Drug Products can be cosmetics, drugs, or both Antimicrobial cleanser Antidandruff shampoo Anticaries toothpaste Antiperspirant-deodorant If it meets the definition of a drug, it must comply with drug requirements even even if it is also a cosmetic No legal definition of cosmeceutical or functional cosmetic OTC Drug vs. Cosmetic OTC Drug Pre-market approval required Safety & efficacy Subject to GMP regulations Establishments & products must be registered No prescription required Symptom relief Cosmetic Pre-market approval not required No pre-market clearance of safety or efficacy GMP guidelines only Establishments & products not required to be registered No prescription required Cleansing, beautifying, or altering the appearance 3

Cosmetics FDA s Authority Cosmetics must not be adulterated or misbranded The law does NOT provide for FDA pre-market approval FDA s authority is post-market only FDA bears the burden of proving a product or ingredient is unsafe before it can act to remove it from the marketplace Appearance standard for Imported products Prohibited Under FD&C Act Adulterated Cosmetics Harmful or injurious under labeled or customary conditions of use Formulation Container Contamination Unapproved Color Additive Coal Tar Hair Dye Exemption (Sec. 601 (a)) Manufactured or held under insanitary conditions Misbranded Cosmetics False or misleading labeling Required information missing or presented improperly Deceptive container Doesn t comply with 1970 Poison Prevention Packaging Act (Child resistant) 4

Cosmetics - Challenges Significant changes in past 5-7 years Manufacturing more global Increasingly sophisticated technology and complex ingredients Nanotechnology Active ingredients Botanicals FDA-Regulated Product Lines Imported Globally 5

Cosmetic Product Lines Imported Globally Hazards and Consequences: Examples Eye Area Cosmetics Microbial Hazards Can be introduced during packaging or repacking Associated with inadequate preservative systems Skin Preparations Microbial Hazards Can be introduced during packaging or repacking Associated with inadequate preservative systems Chemical Hazards Can be introduced during packaging or repacking Wide range of severity in adverse effects 6

Drugs/Cosmetics Recent Situations with Public Health Impact Oral Care Products Alcohol-Free Mouthwash: : regulated as cosmetics or OTC drugs depending on intended use Microbial contamination, severe illnesses, several deaths in one outbreak Products recalled Toothpaste: : diethylene glycol contamination CNS depressant, kidney/liver toxin, vulnerable population Both OTC and cosmetic products detained at U.S. border Recall by distributors and importers Import Alerts for Cosmetics Subject to detention without physical exam Transparent : On FDA Web site Color additives 601(e) Poisonous or deleterious substances - 601(a) Labeling Filth/insanitary conditions Import Alerts: 17-04 - Bulk High-Risk Bovine Tissue from BSE-Countries 66-38 - Skin Care Products with Anti-aging claims 53-06 - Cosmetics Containing Illegal Colors 53-17 - Microbial Contamination of Cosmetics 7

Color Additives Color Additive (21 CFR 70.3 (f)) Synthetic or natural in origin Synthesized, extracted, or isolated Added or applied to food, drug, or the human body Color must be apparent to the naked eye Includes black, white, and intermediate grays Includes food ingredients deliberately used to impart color Does not include food ingredients imparting their own natural color mixed with other foods Color Additives Color Additive Requirements Pre-market approval: chemistry and safety, uses and restrictions Color Additives Exempt From Batch Certification 21 CFR 73 (source: mineral, animal, botanical) Color Additives Subject to Batch Certification 21 CFR 74 (synthetic organic) FDA certification of each batch of certifiable color additive required 8

Newly Listed Color Additive Pearlescent Pigments Mica-based Pearlescent Pigments Exempt from Certification Foods: Final Rule 71 FR 31927, June 2, 2006; Effective Date July 5, 2006 Drugs: Final Rule 70 FR 42273, July 22, 2005; Effective Date August 23, 2005 Pigments prepared from synthetic iron oxide, mica, and titanium dioxide Not listed for use in cosmetics Color Additive Compliance Issues Use of unapproved color additives Use of color additives not approved for use in certain products Use of certified color additives approved for external use only in products like douches and feminine wipes Use of botanical extracts that color the product, but are not approved color additives 9

Color Additive Compliance Issues, cont. Use of Color Index Numbers (CI) alone as color additive designations is NOT permitted for FDA-regulated products marketed in the U.S. Dual Declaration: For products marketed both in U.S. and in EU or other foreign countries that require CI Nos. Examples: FD&C Green No. 3 (CI 42053) Green 3 (CI 42053) Hazards and Consequences Unapproved or uncertified color additives Heavy metals, organic carcinogens potentially high levels Long term exposure potential for severe illness Tissue damage Cancer Neurological damage Potential for widespread consequences because a single lot of color additive may be used in a large number and wide variety of products 10

Import Alerts for Color Additives IA 45-02- Illegal & undeclared color additives IA 53-06- Cosmetics Containing Illegal Colors BSE Many bovine raw materials used in cosmetics Possible vehicle for prion infection Variant Creutzfeldt-Jakob Disease (vcjd) Abraded skin, eye area, mucous membranes 11

BSE in the US No reported cases of vcjd in the US attributed to exposure to US cosmetic products Only BSE case in US traced back to cow of Canadian origin No known cases of cosmetic adulteration with BSE in US or other countries Major efforts continue to assure that food, dietary supplements and cosmetic products remain free from BSE BSE Major Areas of Concern Use of ingredients from high risk TSE tissues (brain, spine/spinal cord, distal ileum, eye) Use of ingredients from ruminants born and raised where BSE or TSE exists Is critical that specific tissue and country of origin is identified for all sources of bovine- derived ingredients Cosmetic industry is a major user of bovine (cow) sources 12

BSE Preventative Measures Safe-sourcing from non-bse countries and certified BSE-free herds Safe processing conditions should be employed - Avoid Co- mingling and cross- contamination Avoid use of high risk material such as brain/spinal cord/eye material Use tallow that has been designated at least Grade III Proposed Record-Keeping for Cosmetics With Cattle Material Federal Register, Vol. 69, No. 134, pgs. 42275-42285, 42285, July 14, 2004 Manufacturers must keep records and make them available to FDA Importers to affirm at time of entry that those cosmetics with cattle material do not contain prohibited material 13

FDA Export Certificates Guidance for cosmetics: http://www.cfsan.fda.gov/~dms/cos-cert.htmlcert.html A certificate is NOT a guarantee nor a certification of the product's safety and quality A certificates does NOT indicate the product or product labeling is approved or sanctioned by the FDA FDA is not required by law to issue export certificates for cosmetics FDA does not require companies to obtain export certificates Thank You For Your Interest! Questions? 14