CRISP APPLE HAND SANI- ethyl alcohol liquid

Crisp Apple Hand Sani by

Drug Labeling and Warnings

Crisp Apple Hand Sani by is a Otc medication manufactured, distributed, or labeled by Walgreen CO, Vi-Jon. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Ethyl Alcohol 65%

Purpose

Antiseptic

Use

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

Warnings

For external use only: hands

Flammable

 Keep away from fire or flame.

When using this product

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

Stop use and ask a doctor if

• irritation and 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 recommed for infants

Other Safety Information

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

Inactive ingredients

benzophenone-4, carbomer, cellulose, fragrance, glycerin, hydroxypropyl methylcellulose, mannitol, red 4, red 40, retinyl palmitate, tocoperyl acetate, ultamarines, water

claims

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

Walgreens Pharmacist Recommended.  Walgreens Pharmacist Survey Study, November 2010

Made in U.S.A. with U.S. and foreign components

Adverse reactions

DISTRIBUTED BY: WALGREEN CO.

200 WILMOT RD., DEERFIELD, IL 60015

100%SATISFACTION GUARANTEED

walgreens.com @2014 Walgreen Co.

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

663.001/663AB

principal display panel

Well at Walgreens

Hand Sanitizer

Crisp Apple

• Kills 99.99% of germs

2 FL OZ (59 mL)

INGREDIENTS AND APPEARANCE

CRISP APPLE HAND SANI 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-0663
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	585 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SULISOBENZONE (UNII: 1W6L629B4K)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
POWDERED CELLULOSE (UNII: SMD1X3XO9M)
GLYCERIN (UNII: PDC6A3C0OX)
HYPROMELLOSES (UNII: 3NXW29V3WO)
MANNITOL (UNII: 3OWL53L36A)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)
FD&C RED NO. 40 (UNII: WZB9127XOA)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ULTRAMARINE BLUE (UNII: I39WR998BI)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-0663-16	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/23/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/23/2014

Labeler - Walgreen CO (008965063)

Registrant - Vi-Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		150931459	manufacture(0363-0663)