FDA.reportPublic FDA data

Alcohol Gel Hand Sanitizer

Manufacturer
Ecolab Inc.
Effective date
2025-12-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:29:39

Label at a glance#

ProductAlcohol Gel Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

For handwashing to decrease bacteria on skin recommended for repeated use

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping. do not use if hands are visibly dirty or greasy; wash hands with soap and water instead.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 60% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic handwash

Uses

INDICATIONS & USAGE SECTION

  • For handwashing to decrease bacteria on skin
  • recommended for repeated use

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

  • In eyes

When using this product

OTC - WHEN USING SECTION

  • If in eyes, rinse promptly and thoroughly with water
  • Discontinue use if irritation and redness develop

Stop use and ask a doctor if

OTC - ASK DOCTOR SECTION

  • skin irritation or redness occurs for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

​Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • wet hands thoroughly with product and allow to dry without wiping.
  • do not use if hands are visibly dirty or greasy; wash hands with soap and water instead.

Other information

REFERENCES SECTION

  • For additional information, see Safety Data Sheet (SDS)

  • EMERGENCY HEALTH INFORMATION: 1 877 231 2615. If located outside the United States and Canada, call collect 952 853 1713 (number is in the US).

Inactive ingredients

INACTIVE INGREDIENT SECTION

​water (aqua), isopropyl alcohol, triethanolamine, acrylates/C10-30 alkyl acrylate crosspolymer, propylene glycol, myristyl alcohol

OTC - QUESTIONS SECTION

Questions? Call 1-800-529-5458

Principal display panel and representative label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ECOLAB

Alcohol Gel Hand Sanitizer

Active Ingredient: Ethyl Alcohol 60% v/v

1200 mL (40.6 US FL OZ)

1112849

Kay Chemical Company · 8300 Capital Drive

Greensboro, NC 27409-9790 USA

Customer Service: (800) 529-5458

©2024 Kay Chemical Company

All rights reserved

KUSA

782984/8000/0224

SDS-NC-872

representative labelrepresentative label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47593-690-70Alcohol Gel Hand Sanitizer1200 mL in 1 BOTTLE, PLASTICSOLUTION12001

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
47593-69047593-690-70

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302IACT
TROLAMINE9O3K93S3TKIACT
CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED)809Y72KV36IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
MYRISTYL ALCOHOLV42034O9PUIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Alcohol Gel Hand SanitizerALCOHOLEcolab Inc.6305da7a-f21c-4e94-a2c1-e1faac489df62025-12-30WarningsExact identifier
ndc (package): 47593-690-70
ndc (product): 47593-690
ndc11 (package): 47593069070
spl id: 6f1d5e34-a74f-4a78-a154-a106f625d4d1
spl set id: 6305da7a-f21c-4e94-a2c1-e1faac489df6

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.