Label: PROPOWER ORIGINALS ANTIMICROBIAL FOAMING SO AP- chloroxylenol liquid
- NDC Code(s): 66294-521-40, 66294-521-42
- Packager: BUNZL
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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Drug Label Information
Updated November 16, 2022
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INGREDIENTS AND APPEARANCE
PROPOWER ORIGINALS ANTIMICROBIAL FOAMING SO AP
chloroxylenol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66294-521 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL 0.005 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) LAURIC ACID (UNII: 1160N9NU9U) MONOETHANOLAMINE (UNII: 5KV86114PT) DIPROPYLENE GLYCOL (UNII: E107L85C40) LACTIC ACID (UNII: 33X04XA5AT) POLOXAMER 124 (UNII: 1S66E28KXA) ISOPROPYL ALCOHOL (UNII: ND2M416302) SODIUM METABISULFITE (UNII: 4VON5FNS3C) SODIUM SULFITE (UNII: VTK01UQK3G) EDETATE SODIUM (UNII: MP1J8420LU) SODIUM SULFATE (UNII: 0YPR65R21J) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLPARABEN (UNII: Z8IX2SC1OH) FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S) D&C RED NO. 33 (UNII: 9DBA0SBB0L) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66294-521-40 1200 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/15/2015 2 NDC:66294-521-42 1250 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/15/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 05/15/2015 Labeler - BUNZL (799540588)