Label: HAND SANITIZER- benzalkonium chloride gel
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Contains inactivated NDC Code(s)
NDC Code(s): 64972-100-01 - Packager: Goodwin Co.
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated January 6, 2021
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Directions
- Keep out of reach of children
- Warnings
- Uses
- Inactive ingredients
- Hand Sanitizer
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INGREDIENTS AND APPEARANCE
HAND SANITIZER
benzalkonium chloride gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64972-100 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.3068 g in 236 mL Inactive Ingredients Ingredient Name Strength CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) WATER (UNII: 059QF0KO0R) COCO GLUCOSIDE (UNII: ICS790225B) COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK) LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64972-100-01 236 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/18/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 03/18/2020 Labeler - Goodwin Co. (183495282) Registrant - Goodwin Co. (183495282) Establishment Name Address ID/FEI Business Operations Goodwin Co. 183495282 manufacture(64972-100)