- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
- Other information
-
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, methylchloroisothizaolinone, CI 19140 (FDC Yellow No. 5), methylisothiazolinone, CI 14700 (FDC Red No. 4)
- QUESTIONS
- Principal display panel and representative label
-
INGREDIENTS AND APPEARANCE
ECOLAB INC.
chloroxylenol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:47593-503 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) GLYCERIN (UNII: PDC6A3C0OX) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) COCO GLUCOSIDE (UNII: ICS790225B) GLYCERYL OLEATE (UNII: 4PC054V79P) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) FD&C RED NO. 4 (UNII: X3W0AM1JLX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:47593-503-41 750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/27/2013 2 NDC:47593-503-59 1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/27/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 10/27/2013 Labeler - Ecolab Inc. (006154611)