FDA.reportPublic FDA data

Ethyl alcohol

Manufacturer
Walmart Inc. | Nice-Pak Products, LLC | Nantong Health & Beyond Hygenic Products, Inc.
Effective date
2026-02-27
Label type
HUMAN OTC DRUG LABEL
Version
18
Source
full-release
Hydrated at
2026-06-01 01:48:12

Label at a glance#

ProductEthyl alcohol
Active ingredientALCOHOL
Label structure13 sections

Indications and uses

to decrease bacteria on the skin that could cause disease recommended for repeated use

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping for children under 6, use only under adult supervision not recommended for infants

Label contents#

Full prescribing information#

active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

purpose

OTC - PURPOSE SECTION

Antiseptic

uses

INDICATIONS & USAGE SECTION

  • to decrease bacteria on the skin that could cause disease
  • recommended for repeated use

Warnings

WARNINGS SECTION

For external use only: hands

Flammable, keep away from fire or flame.

When using this product

OTC - WHEN USING SECTION

  • keep out of eyes.  In case of contact with eyes, flush thoroughly with water.
  • avoid contact with broken skin
  • do ot inhale or ingest

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation and redness develop
  • condition persists for more than 72 hours

Keep out of the reach of children.  

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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
  • for children under 6, use only under adult supervision
  • not recommended for infants

Other information

OTHER SAFETY INFORMATION

  • do not store above 105°F
  • may discolor some fabrics
  • harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, propylene glycol, fragrance, acrylates/C10-30 alkyl acrylate crosspolymer, triethanolamine, blue 1, red 40, yellow 5

Claims

SPL UNCLASSIFIED SECTION

*Effective at eliminating 99.99% of many common harmful germs and bacteria in as little as 15 seconds.

Adverse Reactions

ADVERSE REACTIONS SECTION

DISTRIBUTED BY: Walmart Inc., Bentonville, AR 72716

Product of China

Principal Panel Display

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

49035-418-10

equate™

HAND SANITIZER

Sandalwood & Sea

Kills 99.99% of Germs*

Contains Moisturizers

1 FL OZ (29.5 mL)

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN18
581660ethanol 0.62 ML/ML Topical GelSCD18
581660ethanol 62 % Topical GelSY18

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49035-418-10Ethyl alcohol29.5 mL in 1 PACKAGEGEL29.518

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49035-41849035-418-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
TROLAMINE9O3K93S3TKIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
FD&C RED NO. 40WZB9127XOAIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
ALCOHOL3K9958V90MACTIB

Source Document#

Source XML · Source PDF

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
Ethyl alcoholETHYL ALCOHOLWalmart Inc.f7d9bb83-0b80-458b-9554-8adbe51473e42026-02-27Warnings, Adverse reactionsExact identifier
ndc (package): 49035-418-10
ndc (product): 49035-418
ndc11 (package): 49035041810
spl id: 4bd2e99d-5e97-e02c-e063-6294a90a6555
spl set id: f7d9bb83-0b80-458b-9554-8adbe51473e4

Reported adverse events (FAERS/openFDA)#

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