Label: ECOLAB CLEAN FORCE- chloroxylenol solution
- NDC Code(s): 47593-515-25, 47593-515-41
- Packager: Ecolab Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 12, 2024
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INACTIVE INGREDIENT
Inactive ingredients water (aqua), potassium cocoate, hexylene glycol, sodium sulfate, tetrasodium EDTA, sodium lauryl sulfate, hydroxyethylcellulose, glycerin, cocoglucoside, glyceryl oleate, citric acid, fragrance, methylchloroisothiazolinone, methylisothiazolinone, FD&C red #40, FD&C yellow #5, D&C red #33
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Representative label and principal display panel
MONOGRAM
CLEANING DISPOSABLES
CLEAN FORCE®
ANTIBACTERIAL HAND SOAP
648500
Hand care
8000181
25 FL OZ (750 mL)
H17
Active Ingredient: Chloroxylenol 0.5%
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Manufactured by (c) 2020 Ecolab Distributed by Ecolab - 1 Ecolab USA Inc - All rights US Foods Place - St. Paul MN reserved Rosemont, IL 55102 USA Made in U.S.A. 60018 USA -
INGREDIENTS AND APPEARANCE
ECOLAB CLEAN FORCE
chloroxylenol solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:47593-515 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL 5 mg in 1 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) 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:47593-515-41 750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/03/2015 2 NDC:47593-515-25 800 mL in 1 POUCH; Type 0: Not a Combination Product 08/03/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 08/03/2015 Labeler - Ecolab Inc. (006154611)