Label: BROOKSTONE CLEAR FRESH ADVANCED FOAMING HAND SANITIZER- benzalkonium chloride solution
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Contains inactivated NDC Code(s)
NDC Code(s): 77731-088-01 - Packager: Argento sc by sicura inc.
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated September 17, 2020
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- Active Ingredient(s)
- PURPOSE
- Use
- Warnings
- When using this product
- Stop use and ask a doctor
- Keep out of reach of children
- Directions
- Other information
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BROOKSTONE CLEAR FRESH ADVANCED FOAMING HAND SANITIZER
benzalkonium chloride solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:77731-088 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 SODIUM LAUROAMPHOACETATE (UNII: SLK428451L) COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK) WATER (UNII: 059QF0KO0R) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) GLYCERIN (UNII: PDC6A3C0OX) OLEA EUROPAEA LEAF (UNII: MJ95C3OH47) CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) DISODIUM HEDTA (UNII: KME849MC7A) BENZOPHENONE (UNII: 701M4TTV9O) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:77731-088-01 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 09/17/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 09/17/2020 Labeler - Argento sc by sicura inc. (168718778)