Label: GOJO MILD ANTIBACTERIAL FOAM HAND SP- benzalkonium chloride liquid
- NDC Code(s): 21749-051-53, 21749-051-89, 21749-051-90, 21749-051-97
- Packager: GOJO Industries, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Export only
Drug Label Information
Updated October 3, 2017
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INGREDIENTS AND APPEARANCE
GOJO MILD ANTIBACTERIAL FOAM HAND SP
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21749-051 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Benzalkonium Chloride (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) Benzalkonium Chloride 0.005 mg in 1 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Propylene Glycol (UNII: 6DC9Q167V3) Cocamidopropyl Betaine (UNII: 5OCF3O11KX) PEG-80 Sorbitan Laurate (UNII: 239B50Y732) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) Ethylhexylglycerin (UNII: 147D247K3P) Glycerin (UNII: PDC6A3C0OX) Lauramine Oxide (UNII: 4F6FC4MI8W) POLYQUATERNIUM-10 (10000 MPA.S AT 2%) (UNII: PI1STR9QYH) PHENOXYETHANOL (UNII: HIE492ZZ3T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:21749-051-53 535 mL in 1 PACKAGE; Type 0: Not a Combination Product 05/01/2017 2 NDC:21749-051-97 700 mL in 1 PACKAGE; Type 0: Not a Combination Product 05/01/2017 3 NDC:21749-051-89 1200 mL in 1 PACKAGE; Type 0: Not a Combination Product 05/01/2017 4 NDC:21749-051-90 1250 mL in 1 PACKAGE; Type 0: Not a Combination Product 05/01/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date export only 05/01/2017 Labeler - GOJO Industries, Inc. (004162038) Establishment Name Address ID/FEI Business Operations GOJO Industries, Inc. 036424534 manufacture(21749-051)
