Label: PUREFORCE- benzalkonium chloride solution
- NDC Code(s): 47593-568-41, 47593-568-59
- Packager: Ecolab Inc.
- 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 May 18, 2023
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- Active Ingredient
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INACTIVE INGREDIENT
Inactive ingredients water (aqua), cocamine oxide, hexylene glycol, PEG-180, glycerin, cocamidopropyl PG-dimonium chloride phosphate, myristamine oxide, phenoxyethanol, polyquaternium 7, citric acid, myristamide DIPA, methyl gluceth-20, caprylic/capric glycerides, PEG-12 dimethicone, potassium hydroxide, fragrance, FD&C blue 1
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INGREDIENTS AND APPEARANCE
PUREFORCE
benzalkonium chloride solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:47593-568 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 5 mg in 1 mL Inactive Ingredients Ingredient Name Strength FD&C BLUE NO. 1 (UNII: H3R47K3TBD) POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) METHYL GLUCETH-20 (UNII: J3QD0LD11P) MYRISTIC DIISOPROPANOLAMIDE (UNII: 17DN142CTK) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 900000 MW) (UNII: B70CUU14M9) PHENOXYETHANOL (UNII: HIE492ZZ3T) MYRISTAMINE OXIDE (UNII: J086PM3RRT) COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4) GLYCERIN (UNII: PDC6A3C0OX) POLYETHYLENE GLYCOL 8000 (UNII: Q662QK8M3B) HEXYLENE GLYCOL (UNII: KEH0A3F75J) WATER (UNII: 059QF0KO0R) COCAMINE OXIDE (UNII: QWA2IZI6FI) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:47593-568-59 1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/26/2016 2 NDC:47593-568-41 750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/26/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 07/26/2016 Labeler - Ecolab Inc. (006154611)