EQUI-STAT- benzalkonium chloride solution

Equi-Stat by

Drug Labeling and Warnings

Equi-Stat by is a Otc medication manufactured, distributed, or labeled by Ecolab Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium Chloride, 0.5%

Purpose

Antiseptic handwash

Uses

for handwashing to decrease bacteria on the skin

Warnings

For external use only

Do not use

• in eyes

When using the product

• if in eyes, rinse promptly and thoroughly with water
• discontinue use if irritation and redness develop

Stop use and ask a doctor if skin irritation or redness occurs for more than 72 hours

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• wet hands and apply product
• scrub hands and forearms
• rinse thoroughly and dry

Other information

• for additional information, see Safety Data Sheet (SDS)
• for emergency medical information in USA and Canada, call 1 800 328 0026

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

QUESTIONS

Questions? call 1-866-781-8787

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 Contents

750 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

INGREDIENTS AND APPEARANCE

EQUI-STAT 
benzalkonium chloride solution

Product 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)