Label: CLEANSE- benzalkonium chloride solution
- NDC Code(s): 53329-184-08, 53329-184-74, 53329-184-84
- Packager: Medline Industries, LP
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated May 29, 2024
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INGREDIENTS AND APPEARANCE
CLEANSE
benzalkonium chloride solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53329-184 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) LAURAMINE OXIDE (UNII: 4F6FC4MI8W) EDETATE SODIUM (UNII: MP1J8420LU) GLYCERIN (UNII: PDC6A3C0OX) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) FD&C RED NO. 4 (UNII: X3W0AM1JLX) SULISOBENZONE (UNII: 1W6L629B4K) MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T) LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV) SODIUM BENZOATE (UNII: OJ245FE5EU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:53329-184-84 1000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 09/26/2016 2 NDC:53329-184-08 221 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/01/2021 3 NDC:53329-184-74 1200 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/01/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 09/26/2016 Labeler - Medline Industries, LP (025460908) Registrant - Medline Industries, LP (025460908)