OTC Medication Information: Advanced Gel Hand Sanitizer

ADVANCED GEL HAND SANITIZER- alcohol solution
Ecolab Inc.

Active ingredient

Ethyl Alcohol 62% w/w (equivalent to 70% 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 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

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

Other information

  • for additional information, see Safety Data Sheet (SDS)
  • for emergency medical information in USA, call 1.800.328.0026

Inactive ingredients Water (Aqua), PEG-32, Cetyl Alcohol, Glycerin, Tetrahydroxypropyl Ethylenediamine, Limnanthes Alba Seed Oil , Acrylates Copolymer, Cyclopentasiloxane, Isopropyl Palmitate, Cyclohexasiloxane, t-Butyl Alcohol, Dimethicone, Tocopheryl Acetate, Titanium Dioxide, Aloe Barbadensis Leaf Juice, fragrance, Panthenol, Denatonium benzoate

​Questions? ​ call ​1.866.781.8787

Representative label and principal display panel

NDC 47593-488-41 ECOLAB

Advanced Gel

Hand Sanitizer

CHG Compatible

Active Ingredient: 62% Ethyl Alcohol w/w

(equivalent to 70% v/v)

6000079

Net Contents:

25 US fl oz (750 mL)

This product may be patented: www.ecolab.com/patents

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

© 2022 Ecolab USA Inc · All rights reserved

Made in United States

www.ecolab.com · 755159/8501/0722

SDS-WI-15014

representative label
(click image for full-size original)
representative label
(click image for full-size original)
ADVANCED GEL HAND SANITIZER
alcohol solution
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:47593-488
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (ALCOHOL) ALCOHOL 70 mL in 100 mL
Inactive Ingredients
Ingredient Name Strength
WATER
POLYETHYLENE GLYCOL 1500
CETYL ALCOHOL
GLYCERIN
EDETOL
MEADOWFOAM SEED OIL
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
CYCLOMETHICONE 5
CYCLOMETHICONE 6
ISOPROPYL PALMITATE
TERT-BUTYL ALCOHOL
.ALPHA.-TOCOPHEROL ACETATE
DIMETHICONE
TITANIUM DIOXIDE
ALOE VERA LEAF
PANTHENOL
DENATONIUM BENZOATE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:47593-488-33 118 mL in 1 BOTTLE, PLASTIC None
2 NDC:47593-488-31 540 mL in 1 BOTTLE, PLASTIC None
3 NDC:47593-488-32 1000 mL in 1 BOTTLE, PLASTIC None
4 NDC:47593-488-26 1000 mL in 1 POUCH None
5 NDC:47593-488-56 1200 mL in 1 BOTTLE, PLASTIC None
6 NDC:47593-488-41 750 mL in 1 BOTTLE, PLASTIC None
7 NDC:47593-488-49 37 mL in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC Monograph Drug 505G(a)(3) 11/30/2012
Labeler — Ecolab Inc. (006154611)

Revised: 11/2023 Ecolab Inc.

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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