Label: ANTI-BACTERIAL HAND WARM VANILLA SUGAR- alcohol spray
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Contains inactivated NDC Code(s)
NDC Code(s): 62670-5023-2 - Packager: Bath & Body Works, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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.
Drug Label Information
Updated January 5, 2016
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- USE
- WARNINGS
- WHEN USING THIS PRODUCT
- STOP USE AND ASK A DOCTOR
- FLAMMABLE
- KEEP OUT OF REACH OF CHILDREN
- DIRECTIONS
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INACTIVE INGREDIENTS
Water (Aqua, Eau), Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Cocos Nucifera (Coconut) Fruit Extract, Honey Extract (Mel, Extrait de miel), Olea Europaea (Olive) Fruit Extract, Fragrance (Parfum), PEG-12 Dimethicone, Propylene Glycol, Ethylhexyl Methoxycinnamate, Butyl Methoxydibenzoylmethane, Ethylhexyl Salicylate, Butylene Glycol, 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 sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62670-5023 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 72 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62670-5023-2 56 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 01/05/2016 Labeler - Bath & Body Works, Inc. (878952845)