Label: MCD- chloroxylenol solution
- NDC Code(s): 63146-108-03, 63146-108-10
- Packager: Kay Chemical Company
- 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 11, 2022
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- Active ingredient
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INACTIVE INGREDIENT
Inactive ingredients: water (aqua), potassium cocoate, hexylene glycol, sodium sulfate, tetrasodium EDTA, sodium lauryl sulfate, glycerin, citric acid, coco-glucoside, glyceryl oleate, fragrance, methylchloroisothiazolinone, CI 19140 (FDC Yellow No. 5), methylisothiazolinone, CI 14700 (FDC Red No. 4)
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Principal display panel and representative label
NDC 63146-108-10
Kay®
Peel Here For Drug Facts
McD® Foaming
Antibacterial Hand Soap
Instant foam lathers fast •Mild, pH-balanced formula •Fresh, clean fragrance
McD® Foaming Antibacterial Hand Soap is a rich lather hand soap with a balanced blend of cleaning agents and skin protecting moisturizers.
KEEP OUT OF REACH OF CHILDREN • FOR INSTITUTIONAL USE ONLY
Chloroxylenol 0.5%
To obtain Spanish Instructions, see outer carton.
Net contents: 42 US fl oz (1250 mL)
Distributed by:
KAY CHEMICAL COMPANY•8300 Capital Drive
Greensboro, NC 27409-9790, USA
Customer Service: (800) 529-5458
®2015 Kay Chemical Company
All rights reserved
763982-00•McDUSA 763982/8000/1115
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INGREDIENTS AND APPEARANCE
MCD
chloroxylenol solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63146-108 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 (UNII: 0YPR65R21J) EDETATE SODIUM (UNII: MP1J8420LU) SODIUM LAURYL SULFATE (UNII: 368GB5141J) GLYCERIN (UNII: PDC6A3C0OX) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) GLYCERYL MONOOLEATE (UNII: C4YAD5F5G6) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) FD&C RED NO. 4 (UNII: X3W0AM1JLX) COCO GLUCOSIDE (UNII: ICS790225B) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63146-108-03 750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/17/2007 09/18/2019 2 NDC:63146-108-10 1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/17/2007 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 08/17/2007 Labeler - Kay Chemical Company (003237021)