Label: KAY MCD- chloroxylenol solution
- NDC Code(s): 63146-102-01
- Packager: Kay Chemical Company
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated July 26, 2022
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INGREDIENTS AND APPEARANCE
KAY MCD
chloroxylenol solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63146-102 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL 0.5 mg in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) POTASSIUM COCOATE (UNII: F8U72V8ZXP) HEXYLENE GLYCOL (UNII: KEH0A3F75J) SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750) EDETATE SODIUM (UNII: MP1J8420LU) SODIUM LAURYL SULFATE (UNII: 368GB5141J) HYDROXYETHYL CELLULOSE (3000 MPA.S AT 1%) (UNII: 7Q6P4JN1QT) GLYCERIN (UNII: PDC6A3C0OX) COCO GLUCOSIDE (UNII: ICS790225B) GLYCERYL OLEATE (UNII: 4PC054V79P) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) FD&C RED NO. 40 (UNII: WZB9127XOA) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) D&C RED NO. 33 (UNII: 9DBA0SBB0L) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63146-102-01 3800 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/13/2005 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 10/13/2005 Labeler - Kay Chemical Company (003237021)