Label: 719 WALNUT AVE HAND FRESH ALOE- benzalkonium chloride liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 29500-0555-1 - Packager: Personal Care Products
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated May 21, 2017
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- Official Label (Printer Friendly)
- Drug Factsactive ingredients
- Purpose
- Use
- Warnings
- Stop use and ask a doctor if
- Keep out of reach of children.
- Directions
- Inactive Ingredients
- 719 WALNUT AVE® FOAMING HAND SANITIZER fresh aloe product label
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INGREDIENTS AND APPEARANCE
719 WALNUT AVE HAND FRESH ALOE
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:29500-0555 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 78 mg in 60 mL Inactive Ingredients Ingredient Name Strength CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) DIMETHICONE (UNII: 92RU3N3Y1O) DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M) ALOE VERA LEAF (UNII: ZY81Z83H0X) GLYCERIN (UNII: PDC6A3C0OX) EDETATE DISODIUM (UNII: 7FLD91C86K) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:29500-0555-1 60 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 06/19/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 06/19/2017 Labeler - Personal Care Products (966155082) Registrant - Personal Care Products (966155082)