Label: ZYLAST XP ANTISEPTIC- benzethonium chloride lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 57702-465-01, 57702-465-04, 57702-465-14 - Packager: Bocchi Laboratories Inc.
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated March 31, 2014
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- Keep out of reach of children.
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INGREDIENTS AND APPEARANCE
ZYLAST XP ANTISEPTIC
benzethonium chloride lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:57702-465 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE 2 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) GLYCERIN (UNII: PDC6A3C0OX) POLIHEXANIDE (UNII: 322U039GMF) DIMETHICONE (UNII: 92RU3N3Y1O) STEARAMIDOPROPYL DIMETHYLAMINE (UNII: K7VEI00UFR) BENZYL ALCOHOL (UNII: LKG8494WBH) FARNESOL (UNII: EB41QIU6JL) PANTHENOL (UNII: WV9CM0O67Z) ZINC GLUCONATE (UNII: U6WSN5SQ1Z) CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:57702-465-01 59.1 mL in 1 BOTTLE 2 NDC:57702-465-04 236.6 mL in 1 BOTTLE 3 NDC:57702-465-14 1000 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part333E 06/01/2011 Labeler - Bocchi Laboratories Inc. (078376306)