Label: FRESH HAND FOAMING HAND SANITIZER NON-ALCOHOL FOAM- benzalkonium chloride solution
- NDC Code(s): 70415-204-11
- Packager: CWGC LA Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated September 21, 2023
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INGREDIENTS AND APPEARANCE
FRESH HAND FOAMING HAND SANITIZER NON-ALCOHOL FOAM
benzalkonium chloride solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70415-204 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) COCO GLUCOSIDE (UNII: ICS790225B) LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC) COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70415-204-11 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/05/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 08/05/2020 Labeler - CWGC LA Inc. (034967904)