ECOLAB- benzalkonium chloride solution

Ecolab by

Drug Labeling and Warnings

Ecolab 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 0.55%

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. If located outside the United States and Canada, call collect 1 651 222 5352 (number is in the US)

INACTIVE INGREDIENT

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

Questions? call 1 866 781 8787

Representative Label and Principal Display Panel

ECOLAB®

47593-521-41

EQUI-SOFT™ Foam

ANTIMICROBIAL HAND SOAP

Active Ingredient: 0.55% Benzalkonium Chloride

Antimicrobial Handwash for Healthcare

CHG Compatible

6000149

25 fl oz (750 mL)

Ecolab, St. Paul MN 55102

© 2013 Ecolab USA Inc., All rights reserved

Made in United States, 759869/8500/0814

INGREDIENTS AND APPEARANCE

ECOLAB 
benzalkonium chloride solution

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

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

Inactive Ingredients
Ingredient Name	Strength
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)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
HYDROXYPROPYL GUAR (2500-4500 MPA.S AT 1%) (UNII: 3A1I7376TC)
PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95)
ALCOHOL (UNII: 3K9958V90M)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
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
5	NDC: 47593-521-57	535 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/15/2014

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

Labeler - Ecolab Inc. (006154611)