ECOLAB- alcohol solution

Advanced Gel Hand Sanitizer by

Drug Labeling and Warnings

Advanced Gel Hand Sanitizer 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 62% v/v

Purpose

Antiseptic handwash

Uses

• For handwashing to decrease bacteria on skin

Warnings

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

Do no 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

• 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), PEG-32, cetyl alcohol, glycerin, tetrahydroxyethyl ethylenediamine, meadowfoam seed oil, acrylates/C10-30 alkyl acrylate crosspolymer, cyclopentasiloxane, isopropyl palmitate, cyclohexasiloxane, tert-butyl alcohol, tocopheryl acetate, dimethicone, titanium dioxide, aloe barbadensis leaf juice, panthenol, dentaonium benzoate, fragrance

QUESTIONS

​Questions?​ call ​1 866 781 8787

Principal Display Panel and Representative Label

​​ECOLAB®

NDC: 47593-488-41

Advanced Gel Hand Sanitizer

​CHG Compatible

Active Ingredient: 62% Ethyl Alcohol

6000079

Net Contents: 750 mL (25 fl oz)

Ecolab · 370 Wabasha Street N · St Paul MN 55102-1390 USA
© 2013 Ecolab USA Inc · All rights reserved
Made in United States
755159/8500/0413
SDS-WI-15014

INGREDIENTS AND APPEARANCE

ECOLAB 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47593-488
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)
CETYL ALCOHOL (UNII: 936JST6JCN)
GLYCERIN (UNII: PDC6A3C0OX)
EDETOL (UNII: Q4R969U9FR)
MEADOWFOAM SEED OIL (UNII: 412ZHA4T4Y)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
DIMETHICONE (UNII: 92RU3N3Y1O)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PANTHENOL (UNII: WV9CM0O67Z)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47593-488-33	118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/30/2012	05/01/2018
2	NDC: 47593-488-31	540 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/30/2012
3	NDC: 47593-488-32	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/30/2012
4	NDC: 47593-488-26	1000 mL in 1 POUCH; Type 0: Not a Combination Product	11/30/2012
5	NDC: 47593-488-56	1200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/30/2012
6	NDC: 47593-488-41	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/30/2012
7	NDC: 47593-488-49	37 mL in 1 BOTTLE, PLASTIC; Type 1: Convenience Kit of Co-Package	11/30/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	11/30/2012

Labeler - Ecolab Inc. (006154611)