Label: CHLOROXYLENOL 0.3% liquid
- NDC Code(s): 69842-946-38, 69842-946-57
- Packager: CVS Pharmacy
- Category: HUMAN OTC DRUG LABEL
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 April 20, 2023
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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 3.0 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 not final part333A 01/17/2017 Labeler - CVS Pharmacy (062312574) Registrant - Vi-Jon, LLC (088520668) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(69842-946) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(69842-946)
