Label: SCOTT MOISTURIZING FOAM HAND SANITIZER- alcohol solution
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Contains inactivated NDC Code(s)
NDC Code(s): 55118-703-12 - Packager: Kimberly-Clark Corporation
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated July 22, 2021
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- 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:55118-703 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) PEG-10 Dimethicone (600 CST) (UNII: 8PR7V1SVM0) Betaine (UNII: 3SCV180C9W) PEG-7 Glyceryl Cocoate (UNII: VNX7251543) Meadowfoamamidopropyl Betaine (UNII: HNV0L650LG) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55118-703-12 1200 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 09/01/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 09/01/2015 Labeler - Kimberly-Clark Corporation (830997032)