Label: ANTI-BACTERIAL HAND- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 62670-3643-0, 62670-3643-1, 62670-3643-3 - Packager: Bath & Body Works, Inc.
- Category: HUMAN OTC DRUG LABEL
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.
Drug Label Information
Updated January 1, 2010
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- USE
- WARNINGS
- FLAMMABLE
- KEEP OUT OF REACH OF CHILDREN
- DIRECTIONS
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INACTIVE INGREDIENTS
Water (Aqua, Eau), Isopropyl Alcohol, Fragrance (Parfum), Honey Extract (Mel, Extrait de Miel), Elaeis Guineensis (Palm) Extract, Olea Europaea (Olive) Fruit Extract, Cocos Nucifera (Coconut) Fruit Extract, Wheat Amino Acids, Retinyl Palmitate, Tocopheryl Acetate, Glycerin, Carbomer, Cellulose, Hydroxyethyl Urea, Hydroxypropyl Methylcellulose, Lactose, Isopropyl Myristate, Propylene Glycol, Aminomethyl Propanol, Ultramarines (CI 77007), Yellow 5 (CI 19140), Red 33 (CI 17200), Blue 1 (CI 42090).
- COMPANY INFORMATION
- PRODUCT PACKAGING
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INGREDIENTS AND APPEARANCE
ANTI-BACTERIAL HAND WARM VANILLA SUGAR
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62670-3643 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 68 mL in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62670-3643-0 29 mL in 1 BOTTLE 2 NDC:62670-3643-1 73 mL in 1 BOTTLE 3 NDC:62670-3643-3 236 mL in 1 BOTTLE, PUMP Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 01/01/2010 Labeler - Bath & Body Works, Inc. (878952845)