Label: SCOTT ANTIMICROBIAL FOAM- benzalkonium chloride solution
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Contains inactivated NDC Code(s)
NDC Code(s): 55118-235-10, 55118-235-63 - Packager: Kimberly-Clark
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated October 16, 2019
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- Active Ingredient
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- Inactive Ingredients
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PRINCIPAL DISPLAY PANEL - 33.8 fl oz Bottle Label
Scott®
BrandAntimicrobial Foam Soap
Benzalkonium
Chloride Solution, NFFor Domestic / Personal Care Use
Kills 99.9% of most common germs†
1 Liter
(33.8 fl oz)DIN: 02458675
†Enterococcus faecalis VRE; MDR,
Enterococcus faecium, Pseudomonas aeruginosa,
Escherichia coli, Staphylococcus epidermidis,
Salmonella typhi, Streptococcus pyogenus,
Listeria monocytogenes, Proteus vulgaris,
Salmonella enterica20-29-382-0-01
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INGREDIENTS AND APPEARANCE
SCOTT ANTIMICROBIAL FOAM
benzalkonium chloride solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55118-235 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Benzalkonium Chloride (UNII: F5UM2KM3W7) (Benzalkonium - UNII:7N6JUD5X6Y) Benzalkonium Chloride 1 mg in 1000 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Coco-Betaine (UNII: 03DH2IZ3FY) Glycerin (UNII: PDC6A3C0OX) Sodium Chloride (UNII: 451W47IQ8X) Sodium Benzoate (UNII: OJ245FE5EU) Citric Acid Monohydrate (UNII: 2968PHW8QP) Aloe (UNII: V5VD430YW9) Panthenol (UNII: WV9CM0O67Z) .Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0) Sodium Hydroxide (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55118-235-63 3 in 1 CARTON 12/01/2016 1 NDC:55118-235-10 1000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part333E 12/01/2016 Labeler - Kimberly-Clark (830997032)