Active ingredient

Ethyl Alcohol 62%

Purpose

Antimicrobial

Uses

Hand sanitizer to help reduce bacteria on the skin that could cause disease
Recommended for repeated use

Warnings

Flammable. Keep away from fire or flame.

For external use only

When using this product

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor

if irritation or rash appears and lasts

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
Children under 6 years of age should be supervised when using PURELL

Inactive ingredients

Water (Aqua), Isopropyl Alcohol, Glycerin, Aloe Barbadensis Leaf Juice, Isopropyl Myristate, Propylene Glycol, Retinyl Palmitate, Tocopheryl Acetate, Zea Mays (Corn) Oil

Other information

Store below 110°F (43°C)
May discolor certain fabrics or surfaces

Questions?

Call 1-800-321-0647
www.GOJO.com

Package/Label Principal Display Panel

NDC #21749-367-68

Non-linting, durable, textured wipe.
Removes light soils & dirt.

Purell

ALCOHOL FORMLATION
SANITIZING WIPES
Kills 99.99% of most common germs

Not for retail sale

175 Wipes - 6 in. x 7 in. (15.2 cm x 17.8 cm)

Canister Label

PURELL ALCOHOL FORMULATION
alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	NDC Product Code (Source)	21749-367
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (ALCOHOL)	ALCOHOL	0.62 mL in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER
ISOPROPYL ALCOHOL
GLYCERIN
ALOE VERA LEAF
ISOPROPYL MYRISTATE
PROPYLENE GLYCOL
VITAMIN A PALMITATE
.ALPHA.-TOCOPHEROL ACETATE, D-
CORN OIL

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	NDC	Package Description	Multilevel Packaging
1	21749-367-63	315 mL In 1 CANISTER	None
2	21749-367-68	700 mL In 1 CANISTER	None
3	21749-367-76	4 mL In 1 POUCH	None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	02/24/2012

Labeler - GOJO Industries, Inc. (004162038)

Establishment
Name	Address	ID/FEI	Operations
GOJO Industries, Inc.		036424534	MANUFACTURE

Revised: 07/2012GOJO Industries, Inc.