Label: DR G WHITENING REFORMER BY EGF- arbutin dimethicone cream
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Updated October 1, 2009
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INGREDIENTS AND APPEARANCE
DR G WHITENING REFORMER BY EGF
arbutin dimethicone cream
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43948-4002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARBUTIN (UNII: C5INA23HXF) (ARBUTIN - UNII:C5INA23HXF) ARBUTIN 1 mL in 50 mL DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 2 mL in 50 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:43948-4002-1 50 mL in 1 JAR Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 11/01/2009 Labeler - The Doctor's Cosmetic Inc (687479378) Registrant - The Doctor's Cosmetic Inc (687479378) Establishment Name Address ID/FEI Business Operations The Doctor's Cosmetic Inc 687479378 manufacture