Label: CHLOROXYLENOL 0.3% liquid
- NDC Code(s): 69842-946-38, 69842-946-57
- Packager: CVS Pharmacy
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated August 7, 2024
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- Official Label (Printer Friendly)
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- Active ingredient
- Purpose
- Use
- Warnings
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
- Directions
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Inactive ingredients
water, sodium C14-16 olefin sulfonate, lauramine oxide or lauramidopropylamine oxide and myristamidopropylamine oxide, sodium laureth sulfate, sodium lauryl sulfate, sodium chloride, sodium xylenesulfonate, alcohol denat., fragrance, phenoxyethanol, citric acid, methylisothiazolinone, tetrasodium EDTA, yellow 5, blue 1
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INGREDIENTS AND APPEARANCE
CHLOROXYLENOL 0.3%
chloroxylenol 0.3% liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-946 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL 3 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U) LAURAMINE OXIDE (UNII: 4F6FC4MI8W) LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV) MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) SODIUM LAURYL SULFATE (UNII: 368GB5141J) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM XYLENESULFONATE (UNII: G4LZF950UR) ALCOHOL (UNII: 3K9958V90M) PHENOXYETHANOL (UNII: HIE492ZZ3T) CITRIC ACID ACETATE (UNII: DSO12WL7AU) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) EDETATE SODIUM (UNII: MP1J8420LU) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69842-946-57 1183 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 01/17/2017 2 NDC:69842-946-38 1123 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 01/17/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 01/17/2017 Labeler - CVS Pharmacy (062312574) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091520 manufacture(69842-946) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(69842-946)