![PURELL SF607 FOAM HAND RUB BENZALKONIUM CHLORIDE SOLUTION NON ALCOHOL (BENZALKONIUM CHLORIDE) LIQUID [GOJO INDUSTRIES, INC.]](https://medic.hrt.org//dailymed/images/f87d8342-d00c-4905-a679-ade010f65425/1eef03c5-2c59-494c-9aaf-a845d273f5ab.jpg)
| NDC | 21749-689-89 |
| Set ID | f87d8342-d00c-4905-a679-ade010f65425 |
| Category | HUMAN OTC DRUG LABEL |
| Packager | GOJO Industries, Inc. |
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INGREDIENTS AND APPEARANCE
PURELL SF607 FOAM HAND RUB BENZALKONIUM CHLORIDE SOLUTION NON ALCOHOL
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21749-689 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:21749-689-89 1200 mL in 1 BOTTLE; Type 0: Not a Combination Product 09/15/2013 01/01/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date export only 09/15/2013 01/01/2024 Labeler - GOJO Industries, Inc. (004162038) Establishment Name Address ID/FEI Business Operations GOJO Industries, Inc. 036424534 manufacture(21749-689)
