Label: EQUI-STAT- benzalkonium chloride solution
- NDC Code(s): 47593-585-31, 47593-585-41, 47593-585-59
- 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 October 18, 2022
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- Active ingredient
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INACTIVE INGREDIENT
Inactive ingredients water (aqua), cocamine oxide, hexylene glycol, PEG-180, glycerin, hydroxyethylcellulose, cocamidopropyl PG-dimonium chloride phosphate, phenoxyethanol, myristamide DIPA, myristamine oxide, methyl gluceth-20, glyceryl caprylate/caprate, alcohol, PEG-12 dimethicone, citric acid, polyquatemium-7, fragrance, potassium hydroxide, blue 1
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Principal display panel and representative label
NDC 47593-585-41 ECOLAB
EQUI-STAT ™
Antimicrobial Hand Soap
Active Ingredient: 0.5% Benzalkonium Chloride
Antimicrobial Handwash for Healthcare
CHG Compatible
Net Contents750 mL (25 US fl oz) 6000234
This product may be patented | Este producto puede ser patentado: www.ecolab.com/patents
Ecolab · 1 Ecolab Place · St. Paul MN 55102 USA · tel: 1 800 35 CLEAN (352 5326)
© 2017 Ecolab USA Inc. · All rights reserved | Todos los derechos reservados
Made in U.S.A. | Hecho en EE.UU.
www.ecolab.com · 771525/8500/1017
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INGREDIENTS AND APPEARANCE
EQUI-STAT
benzalkonium chloride solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:47593-585 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 WATER (UNII: 059QF0KO0R) COCAMINE OXIDE (UNII: QWA2IZI6FI) HEXYLENE GLYCOL (UNII: KEH0A3F75J) POLYETHYLENE GLYCOL 8000 (UNII: Q662QK8M3B) GLYCERIN (UNII: PDC6A3C0OX) HYDROXYETHYL CELLULOSE (4000 MPA.S AT 1%) (UNII: ZYD53NBL45) COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4) PHENOXYETHANOL (UNII: HIE492ZZ3T) MYRISTIC DIISOPROPANOLAMIDE (UNII: 17DN142CTK) MYRISTAMINE OXIDE (UNII: J086PM3RRT) METHYL GLUCETH-20 (UNII: J3QD0LD11P) GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N) ALCOHOL (UNII: 3K9958V90M) PEG-12 DIMETHICONE (UNII: ZEL54N6W95) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y) POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:47593-585-31 540 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/20/2017 2 NDC:47593-585-59 1250 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/20/2017 3 NDC:47593-585-41 750 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/20/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 12/20/2017 Labeler - Ecolab Inc. (006154611)