NDC | 21749-855-53, 21749-855-90 |
Set ID | 63c5e172-2f0a-4c0f-81d7-d3edca3e21d9 |
Category | HUMAN OTC DRUG LABEL |
Packager | GOJO Industries, Inc. |
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- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PURELL SF607 ALCOHOL FREE INSTANT HAND SANITIZER FOAM
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21749-855 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.0013 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) METHYLPARABEN (UNII: A2I8C7HI9T) PHENOXYETHANOL (UNII: HIE492ZZ3T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:21749-855-53 535 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/30/2014 01/01/2024 2 NDC:21749-855-90 1250 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/15/2013 01/01/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date export only 05/15/2013 01/01/2024 Labeler - GOJO Industries, Inc. (004162038) Establishment Name Address ID/FEI Business Operations GOJO Industries, Inc. 036424534 manufacture(21749-855)