Alcohol

Manufacturer
Walgreen Co. | Nice-Pak Products, LLC
Effective date
2026-02-12
Label type
HUMAN OTC DRUG LABEL
Version
14
Source
full-release
Hydrated at
2026-06-01 01:44:04

Label at a glance#

ProductAlcohol
Active ingredientALCOHOL
Label structure12 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 not inhale of 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 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, carbomer, fragrance, glycerin, isopropyl myristate, Aloe barbadensis leaf juice, tocopheryl acetate, blue 1, yellow 5

ADVERSE REACTION

ADVERSE REACTIONS SECTION

Walgreens Pharmacist Recommended

Walgreens Pharmacist Survey

*Effective at eliminating 99.99% of many common harmful germs and bacteria in as little as 15 seconds. See Walgreens.com for details.

DISTRIBUTED BY: WALGREEN CO.

200 WILMOT RD., DEERFIELD, IL 60015

100% SATISFACTION GUARANTEED

walgreens.com.  ©2020 Walgreen Co.

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Walgreens

Hand Sanitizer

ETHYL ALCOHOL 62% / ANTISEPTIC

  • Kills 99.99% of germs*
  • With moisturizers to leave hands feeling smooth

2 FL OZ (59 mL)

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
247835ethanol 62 % Topical SolutionPSN14
247835ethanol 0.62 ML/ML Topical SolutionSCD14
247835ethanol 62 % Topical SolutionSY14
247835ethyl alcohol 62 % Topical SolutionSY14

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-0046-16Alcohol59 mL in 1 BOTTLE, PLASTICLIQUID5914

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-00460363-0046-16

Ingredients#

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

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

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
AlcoholALCOHOLWalgreen Co.1e879904-055e-4bec-a504-3c783fc9fb242026-02-12Warnings, Adverse reactionsExact identifier
ndc (package): 0363-0046-16
ndc (product): 0363-0046
ndc11 (package): 00363004616
spl id: 4aa55b68-0251-e9b8-e063-6394a90aebae
spl set id: 1e879904-055e-4bec-a504-3c783fc9fb24

Reported adverse events (FAERS/openFDA)#

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