Label: NU SKIN EPOCH- alcohol gel
- 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 December 14, 2009
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- Active Ingredient
- Inactive Ingredients
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 100 mL Bottle Label
INGREDIENTS AND APPEARANCE
NU SKIN EPOCH
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:12488-1800 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol 61.9937 mL in 100 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Polyoxyl 40 Hydrogenated Castor Oil (UNII: 7YC686GQ8F) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:12488-1800-1 100 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH FINAL part333 06/01/2009 Labeler - Alberto-Culver USA Inc. (021679448) Establishment Name Address ID/FEI Business Operations Alberto-Culver USA Inc. 021679448 ANALYSIS, MANUFACTURE