Label: ANTIMICROBIAL HAND WASH- benzalkonium chloride soap
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Contains inactivated NDC Code(s)
NDC Code(s): 78902-103-16, 78902-103-25, 78902-103-32 - Packager: Jocott Brands, Inc.
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated June 27, 2020
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- ACTIVE INGREDIENT
- PURPOSE
- USE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- DIRECTIONS
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INACTIVE INGREDIENTS
PURIFIED WATER (AQUA), SODIUM LAURETH SULFATE, COCAMIDOPROPYL BETAINE, SODIUM CHLORIDE, ALOE BARBADENSIS (ALOE VERA) LEAF JUICE, COCOS NUCIDERA (COCONUT) OIL, ARGANIA SPINOSA (ARGAN) KERNEL OIL, SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL, BUTYROSPERMUM PARKII (SHEA) BUTTER, CUCUMIS SATIVUS (CUCUMBER) FRUIT EXTRACT, GLYCERIN, POLYQUATERNIUM-7, PEG-150 DISTEARATE, PHENOXYETHANOL, DEHYDROACETIC ACID, BENZYL ALCOHOL, FRAGRANCE (PARFUM)
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ANTIMICROBIAL HAND WASH
benzalkonium chloride soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:78902-103 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 WATER (UNII: 059QF0KO0R) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) SODIUM CHLORIDE (UNII: 451W47IQ8X) ALOE VERA LEAF (UNII: ZY81Z83H0X) COCONUT OIL (UNII: Q9L0O73W7L) ARGAN OIL (UNII: 4V59G5UW9X) JOJOBA OIL (UNII: 724GKU717M) SHEA BUTTER (UNII: K49155WL9Y) CUCUMBER (UNII: YY7C30VXJT) GLYCERIN (UNII: PDC6A3C0OX) POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y) PEG-150 DISTEARATE (UNII: 6F36Q0I0AC) PHENOXYETHANOL (UNII: HIE492ZZ3T) DEHYDROACETIC ACID (UNII: 2KAG279R6R) BENZYL ALCOHOL (UNII: LKG8494WBH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:78902-103-16 480 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/27/2020 2 NDC:78902-103-32 960 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/27/2020 3 NDC:78902-103-25 750 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/27/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 06/27/2020 Labeler - Jocott Brands, Inc. (080399826)