Label: HAND WASH- benzalkonium chloride liquid
- NDC Code(s): 63940-575-45
- Packager: Harmon Stores, Inc
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated June 28, 2022
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- Active ingredient
- Purpose
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- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children
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- Inactive ingredients
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INGREDIENTS AND APPEARANCE
HAND WASH
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63940-575 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE .999 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV) LAURAMINE OXIDE (UNII: 4F6FC4MI8W) MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T) GLYCERIN (UNII: PDC6A3C0OX) LINALOOL, (+/-)- (UNII: D81QY6I88E) BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69) LIMONENE, (+/-)- (UNII: 9MC3I34447) GERANIOL (UNII: L837108USY) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) EDETATE SODIUM (UNII: MP1J8420LU) SULISOBENZONE (UNII: 1W6L629B4K) SODIUM BENZOATE (UNII: OJ245FE5EU) D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63940-575-45 946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/04/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/04/2016 Labeler - Harmon Stores, Inc (804085293) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(63940-575) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(63940-575)