ECOLAB- alcohol 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

Ethyl Alcohol 70% w/w

Purpose

Antiseptic handwash

Uses

• For handwashing to decrease bacteria on the skin
• Recommended for repeated use

Warnings

• For external use only
• Flammable, keep away from fire or flame, sparks and sources of static discharge

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 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

• Apply product onto hands, spread thoroughly and rub until dry

Other information

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

INACTIVE INGREDIENT

Inactive ingredients water (aqua), glycerin, acrylates/C10-30 alkyl acrylate crosspolymer, tetrahydroxyethyl ethylenediamine, cetearyl methicone, C12-C15 alkyl benzoate, ethylhexylglycerin, dimethicone, cetyl alcohol, tocopheryl acetate, dicaprylyl caprylate, tert-butyl alcohol, fragrance, dentaonium benzoate

QUESTIONS

Questions? call 1 866 781 8787

Principal Display Panel and Representative Label

ECOLAB®

NDC: 47593-502-31

Express Gel

Hand Sanitizer

Dye Free

CHG Compatible

Active Ingredient: 70% Ethyl Alcohol

6000057

Net Contents:

540 mL (18 fl oz)

Ecolab · 370 Wabasha Street N · St Paul MN 55102-1390 USA

© 2013 Ecolab USA Inc · All rights reserved

Made in United States

754494/8500/0113

SDS-WI-15014

INGREDIENTS AND APPEARANCE

ECOLAB 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47593-502
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	598.5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
ETHYLENEDIAMINE TETRAETHANOL (UNII: K5APE098ZI)
FERUMOXSIL (UNII: 6HJV9H13XS)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
DIMETHICONE (UNII: 92RU3N3Y1O)
CETYL ALCOHOL (UNII: 936JST6JCN)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47593-502-31	540 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/26/2013
2	NDC: 47593-502-49	37 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/26/2013
3	NDC: 47593-502-58	15 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/26/2013
4	NDC: 47593-502-33	118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/26/2013
5	NDC: 47593-502-41	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/26/2013
6	NDC: 47593-502-56	1200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/26/2013

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/26/2013

Labeler - Ecolab Inc. (006154611)