Label: ANTI BACTERIAL HAND GEL PUMPKIN APPLE- alcohol gel
- NDC Code(s): 62670-6902-3
- Packager: Bath & Body Works, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 10, 2026
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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
Water (Aqua, Eau), Fragrance (Parfum), Carbomer, Mannitol, Isopropyl Myristate, Cellulose, Hydroxyethyl Urea, Tocopheryl Acetate, Wheat Amino Acids, Aloe Barbadensis Leaf Juice, Butyrospermum Parkii (Shea) Butter Extract, Silica, Kaolin, Retinyl Palmitate, Caprylic/Capric Triglyceride, Hydroxypropyl Methylcellulose, Aminomethyl Propanol, Ultramarines (CI 77007), Yellow 6 (CI 15985), Red 4 (CI 14700), Yellow 5 (CI 19140), Blue 1 (CI 42090).
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ANTI BACTERIAL HAND GEL PUMPKIN APPLE
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62670-6902 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:62670-6902-3 225 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/04/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 08/04/2025 Labeler - Bath & Body Works, Inc. (878952845) Establishment Name Address ID/FEI Business Operations MCP TN, LLC 118929829 manufacture(62670-6902)

