Label: SCOTT MOISTURIZING FOAM HAND SANITIZER- alcohol solution
- NDC Code(s): 55118-546-10, 55118-546-12, 55118-546-63, 55118-546-65
- Packager: Kimberly-Clark
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 12, 2024
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 1.2 Liter Bottle Label
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INGREDIENTS AND APPEARANCE
SCOTT MOISTURIZING FOAM HAND SANITIZER
alcohol solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55118-546 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol 62 mL in 100 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Betaine (UNII: 3SCV180C9W) Meadowfoamamidopropyl Betaine (UNII: HNV0L650LG) PEG-7 GLYCERYL COCOATE (UNII: VNX7251543) PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55118-546-63 6 in 1 CARTON 04/16/2018 1 NDC:55118-546-10 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:55118-546-65 2 in 1 CARTON 04/16/2018 2 NDC:55118-546-12 1200 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph drug M003 04/16/2018 Labeler - Kimberly-Clark (830997032)