Label: ENRICHED FOAM ALCOHOL-FREE HAND SANITIZER- benzalkonium chloride liquid
- NDC Code(s): 65321-039-01, 65321-039-02, 65321-039-03
- Packager: Rubbermaid Commercial Products LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 18, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
- Use
- Warnings
- Directions
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Inactive Ingredients
Water (Aqua), Propylene Glycol, PEG-6 Caprylic/Capric Glycerides, Phenoxyethanol, Decylamine Oxide, Tetrasodium Glutamate Diacetate, Sodium Hydroxide, Caprylyl Glycol, Ethylhexylglycerin, Lactic Acid, Shea Butteramidopropyl Betaine, Sodium Chloride, Hexylene Glycol, Benzoic Acid, Tocopherol, Sodium Citrate
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 1100 mL Pouch Label
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INGREDIENTS AND APPEARANCE
ENRICHED FOAM ALCOHOL-FREE HAND SANITIZER
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:65321-039 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 13 mg in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) CAPRYLOCAPROYL POLYOXYLGLYCERIDES 6 (UNII: GO50W2HWO8) PHENOXYETHANOL (UNII: HIE492ZZ3T) DECYLAMINE OXIDE (UNII: G387VUT5EZ) TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY) SODIUM HYDROXIDE (UNII: 55X04QC32I) CAPRYLYL GLYCOL (UNII: 00YIU5438U) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT) SODIUM CHLORIDE (UNII: 451W47IQ8X) HEXYLENE GLYCOL (UNII: KEH0A3F75J) BENZOIC ACID (UNII: 8SKN0B0MIM) .ALPHA.-TOCOPHEROL, D- (UNII: N9PR3490H9) SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65321-039-01 4 in 1 BOX 06/21/2021 1 1100 mL in 1 POUCH; Type 0: Not a Combination Product 2 NDC:65321-039-02 4 in 1 BOX 06/21/2021 2 1300 mL in 1 POUCH; Type 0: Not a Combination Product 3 NDC:65321-039-03 6 in 1 BOX 06/21/2021 3 800 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH DRUG M004 06/21/2021 Labeler - Rubbermaid Commercial Products LLC (049924368) Establishment Name Address ID/FEI Business Operations NWL Netherlands Services B.V. 494692088 ANALYSIS(65321-039) , MANUFACTURE(65321-039)