Label: BROOKSTONE LEMON ZEST ADVANCED FOAMING HAND SANITIZER- benzalkonium chloride solution
-
Contains inactivated NDC Code(s)
NDC Code(s): 77731-087-01 - Packager: Argento sc by sicura inc.
- 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 September 17, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- 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
Water, Sodium lauroamphoacetate, Cocamidopropylamine oxide, Cocamidopropyl betaine, Glycerin, Olea europaea (olive) leaf extract, Polyminopropyl biguanide, Citric acid, Disodium EDTA, Benzophenone-3, Methylchloroisothiazolinone, Methylisothiazolinone, Fragrance, Cetylpyridinium chloride, Yellow 5 (CI19140)
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
BROOKSTONE LEMON ZEST ADVANCED FOAMING HAND SANITIZER
benzalkonium chloride solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:77731-087 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) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) 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:77731-087-01 500 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)