Hand Sanitizer: Package Insert and Label Information

HAND SANITIZER- alcohol gel
Walgreens

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Active ingredient

Ethyl alcohol 63%

Purpose

Antiseptic

Uses

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

Warnings

For external use only: hands

Flammable

Keep away from heat and flame

when using this product

  • keep out of eyes. Incase of contact with eyes, flush thoroughly with water
  • avoid contact with broken skin
  • do not inhale or ingest

Stop use and ask a doctor

  • if skin irritation or redness develops
  • condition persists 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

  • 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

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

Inactive ingredients

water, glycerin, tocopheryl acetate, retinyl palmitate, carbomer, fragrance, benzophenone-4, mannitol, cellulose, hydroxypropyl methylcellulose, ultamarines

claims

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

100% SATISFACTION GUARANTEED

walgreens.com

MADE IN U.S.A. WITH US AND FOREIGN COMPONENTS

principal display panel

Well

Walgreens

Hand

Sanitizer

Coconut

water scent

  • Kills 99.99% of germs

2 FL OZ (59 mL)

image description
(click image for full-size original)
HAND SANITIZER
ethyl alcohol gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0469
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (ALCOHOL) ALCOHOL 545 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER
GLYCERIN
.ALPHA.-TOCOPHEROL ACETATE
VITAMIN A PALMITATE
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
SULISOBENZONE
MANNITOL
CELLULOSE ACETATE
HYPROMELLOSES
ULTRAMARINE BLUE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0363-0469-16 59 mL in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 01/26/2015
Labeler — Walgreens (008965063)
Registrant — Vi-Jon, LLC (790752542)
Establishment
Name Address ID/FEI Operations
Vi-Jon, LLC 088520668 manufacture (0363-0469)

Revised: 06/2022 Walgreens

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