Active ingredient

Benzalkonium Chloride 0.55%

Purpose

Antiseptic handwash

Uses

for handwashing to decrease bacteria on the skin

Warnings

For external use only

Do not use

In eyes

When using this 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 skin and spread a small amount on hands and forearms
scrub well, 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
for emergency medical information worldwide, call 1 651 222 5352

Inactive ingredients

water (aqua), hexylene glycol, cocamine oxide, PEG-180, glycerin, cocamidopropyl PG-dimonium chloride phosphate, methyl gluceth-20, phenoxyethanol, myristamide DIPA, caprylic/capric glycerides, citric acid, hydroxypropyl guar hydroxypypropyltrimonium chloride, PEG-12 dimethicone, ethanol, tocopheryl acetate, fragrance, potassium hydroxide

Questions? call 1 866 781 8787

Representative Label and Principal Display Panel

47593-521-59

ECOLAB®

EQUI-SOFT™ Foam

ANTIMICROBIAL HAND SOAP

Active Ingredient: 0.55% Benzalkonium Chloride

Antimicrobial Handwash for Healthcare

CHG Compatible

6000143

1250 mL (42.3 US fl oz)

Ecolab · 1 Ecolab Place · St. Paul MN 55102 USA

www.ecolab.com · 759864/8501/0322

representative label

ECOLAB
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47593-521
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	5.5 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
COCAMINE OXIDE (UNII: QWA2IZI6FI)
POLYETHYLENE GLYCOL 8000 (UNII: Q662QK8M3B)
GLYCERIN (UNII: PDC6A3C0OX)
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
METHYL GLUCETH-20 (UNII: J3QD0LD11P)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
MYRISTIC DIISOPROPANOLAMIDE (UNII: 17DN142CTK)
GLYCERYL CAPRYLOCAPRATE (UNII: U72Q2I8C85)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
GUAR GUM (UNII: E89I1637KE)
PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95)
ALCOHOL (UNII: 3K9958V90M)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:47593-521-59	1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/15/2014
2	NDC:47593-521-41	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/15/2014
3	NDC:47593-521-56	1200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/15/2014
4	NDC:47593-521-38	500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/15/2014	04/03/2023
5	NDC:47593-521-57	535 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/15/2014

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	09/15/2014

Labeler - Ecolab Inc. (006154611)

Drug Facts