FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Walgreen CO. | Vi-Jon, LLC
Effective date
2021-02-12
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 22:52:54

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure14 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 63%

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

SPL UNCLASSIFIED SECTION

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
  • recommended for repeated use

Stop use and ask a doctor

OTC - STOP USE SECTION

  • if 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

SPL UNCLASSIFIED SECTION

  • do not store above 105⁰F
  • may discolor some fabrics
  • harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, tocopheryl acetate, retinyl palmitate, acrylates/C10-30 alkyl acrylate crosspolymer, benzophenone-4, mannitol, cellulose, hydroxypropyl methylcellulose, fragrance, yellow 5, red 4, ultramarines

claims

SPL UNCLASSIFIED SECTION

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

Questions or comments? 1-800-925-4733

adverse reactions section

DISTRIBUTED BY:WALGREEN CO.

200 WILMOT RD., DEERFIELD, IL 60015

1005 SATISFACTION GUARANTEED

walgreens.com

297.000/297AA

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Well at Walgreens

NEW

Hand

Sanitizer

Fresh Tangerine Scent

Kills 99.99% of germs

2 FL OZ (59 mL)

image descriptionimage description

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-08260363-0826-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
glycerinPDC6A3C0OXIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
VITAMIN A PALMITATE1D1K0N0VVCIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
SULISOBENZONE1W6L629B4KIACT
MANNITOL3OWL53L36AIACT
POWDERED CELLULOSESMD1X3XO9MIACT
HYPROMELLOSES3NXW29V3WOIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
FD&C RED NO. 4X3W0AM1JLXIACT
ULTRAMARINE BLUEI39WR998BIIACT

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
081d589f-b3e5-47b3-90ca-a955dad6322ba3a2b40a-90ec-4fc9-a129-69cded7d083d2022-02-04Warnings, Adverse reactionsExact identifier
spl set id: a3a2b40a-90ec-4fc9-a129-69cded7d083d

Reported adverse events (FAERS/openFDA)#

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