Label: ANTI-BACTERIAL HAND GEL FROSTED CRANBERRY- alcohol gel
- NDC Code(s): 62670-6572-0
- Packager: Bath & Body Works, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 20, 2023
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- Active Ingredient
- Purpose
- Use
- Warnings
- WARNINGS
- WHEN USING
- KEEP OUT OF REACH OF CHILDREN
- Directions
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INACTIVE INGREDIENT
Inactive Ingredients Water (Aqua, Eau), Fragrance (Parfum), Propylene Glycol, Carbomer, Aminomethyl Propanol, Isopropyl Myristate, Hydroxyethyl Urea, Wheat Amino Acids, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Butyrospermum Parkii (Shea) Butter Extract, Red 33 (CI 17200), Red 40 (CI 16035), Blue 1 (CI 42090), Yellow 5 (CI 19140), Ext. Violet 2 (CI 60730).
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INGREDIENTS AND APPEARANCE
ANTI-BACTERIAL HAND GEL FROSTED CRANBERRY
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62670-6572 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 71 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:62670-6572-0 29 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/28/2023 08/28/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 08/28/2023 08/28/2025 Labeler - Bath & Body Works, Inc. (878952845) Establishment Name Address ID/FEI Business Operations KDC US Holdings, Inc. 080783283 manufacture(62670-6572) Establishment Name Address ID/FEI Business Operations Memphis Contract Packaging 117443103 manufacture(62670-6572)