Label: TRITON AB-741- chloroxylenol soap
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Contains inactivated NDC Code(s)
NDC Code(s): 65601-741-62 - Packager: Betco Corporation, Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated November 12, 2012
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- Official Label (Printer Friendly)
- Triton AB-741
- Triton AB-741
- Triton AB-741
- Triton AB-741
- Triton AB-741
- Triton AB-741
- Triton AB-741
- Triton AB-741
- Triton AB-741
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INGREDIENTS AND APPEARANCE
TRITON AB-741
chloroxylenol soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:65601-741 Route of Administration Topical Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL 3.75 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM LAURYL SULFATE (UNII: 368GB5141J) COCO DIETHANOLAMIDE (UNII: 92005F972D) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) PHENOXYETHANOL (UNII: HIE492ZZ3T) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) DMDM HYDANTOIN (UNII: BYR0546TOW) GLYCOL STEARATE (UNII: 0324G66D0E) LAURIC DIETHANOLAMIDE (UNII: I29I2VHG38) GLYCERIN (UNII: PDC6A3C0OX) D&C GREEN NO. 5 (UNII: 8J6RDU8L9X) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65601-741-62 2000 mL in 1 BOTTLE, DISPENSING Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 11/12/2012 Labeler - Betco Corporation, Ltd. (005050158) Registrant - Betco corporation, Ltd. (005050158) Establishment Name Address ID/FEI Business Operations Betco Corpo, Ltd. 005050158 manufacture(65601-741)