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
- 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 July 13, 2023
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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 not final part333E 04/16/2018 Labeler - Kimberly-Clark (830997032)