Label: SAN-X E2- benzalkonium chloride liquid
- NDC Code(s): 69884-707-06
- Packager: Amerisan, LLC
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated January 31, 2022
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INGREDIENTS AND APPEARANCE
SAN-X E2
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69884-707 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.12 mg in 100 mL Inactive Ingredients Ingredient Name Strength EDETIC ACID (UNII: 9G34HU7RV0) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYETHYLENE GLYCOL 800 (UNII: UH6KR4953D) BENZYL ALCOHOL (UNII: LKG8494WBH) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) DEHYDROACETIC ACID (UNII: 2KAG279R6R) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69884-707-06 1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/19/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 02/19/2016 12/31/2024 Labeler - Amerisan, LLC (170260090) Establishment Name Address ID/FEI Business Operations Best Sanitizers 627278224 manufacture(69884-707)