Label: HYDRO KLEEN AF- benzalkonium chloride liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 69129-010-01 - Packager: Productive Practices
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated August 1, 2014
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- PRINCIPAL DISPLAY PANEL - 200 mL Bottle Label
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INGREDIENTS AND APPEARANCE
HYDRO KLEEN AF
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69129-010 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 1 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Polysorbate 20 (UNII: 7T1F30V5YH) Glycerin (UNII: PDC6A3C0OX) Citric Acid Monohydrate (UNII: 2968PHW8QP) Butylene Glycol (UNII: 3XUS85K0RA) Cocamidopropylamine Oxide (UNII: M4SL82J7HK) Sodium Hydroxide (UNII: 55X04QC32I) Cocamidopropyl Betaine (UNII: 5OCF3O11KX) CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69129-010-01 200 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part333E 07/31/2014 Labeler - Productive Practices (010122499)