Label: FOAMING HAND SANITIZER REFILL MOISTURIZING ALOE- benzalkonium chloride liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 81527-001-16, 81527-001-32 - Packager: Bocks Inc
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated February 8, 2021
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredient
- Uses
- Warnings
- Directions
- Inactive Ingredients
- Package Labeling: 473ml
- Package Labeling: 946ml
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INGREDIENTS AND APPEARANCE
FOAMING HAND SANITIZER REFILL MOISTURIZING ALOE
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81527-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) HYDROXYPROPYL BIS-HYDROXYETHYLDIMONIUM CHLORIDE (UNII: 1EO3O1X7HG) SODIUM CITRATE (UNII: 1Q73Q2JULR) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81527-001-16 473 mL in 1 CARTON; Type 0: Not a Combination Product 02/01/2021 2 NDC:81527-001-32 946 mL in 1 CARTON; Type 0: Not a Combination Product 02/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 02/01/2021 Labeler - Bocks Inc (082200343)