PURELL HAND SANITIZING WIPES ALCOHOL FORMULA- alcohol cloth
GOJO Industries, Inc.

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.

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PURELL Hand Sanitizing Wipes Alcohol Formula

Active ingredient

Ethyl alcohol 62%

Purpose

Antimicrobial

Use

Hand sanitizer to help reduce bacteria on the skin

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® products

Other information

• Store below 110°F (43°C)

• May discolor certain fabrics or surfaces

Inactive ingredients

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

Product Label

PURELL HAND SANITIZING WIPES ALCOHOL FORMULA
alcohol cloth

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

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CORN OIL (UNII: 8470G57WFM)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:21749-367-76	1 in 1 PACKAGE	02/24/2012	12/31/2019
1		1.97 mL in 1 POUCH; Type 0: Not a Combination Product
2	NDC:21749-367-24	24 in 1 PACKAGE	02/24/2012	12/31/2019
2		66 mL in 1 PACKAGE; Type 0: Not a Combination Product
3	NDC:21749-367-36	36 in 1 PACKAGE	02/24/2012
3		101 mL in 1 PACKAGE; Type 0: Not a Combination Product
4	NDC:21749-367-63	80 in 1 PACKAGE	02/24/2012
4		219 mL in 1 CANISTER; Type 0: Not a Combination Product
5	NDC:21749-367-94	135 in 1 PACKAGE	02/24/2012	12/31/2019
5		370 mL in 1 PACKAGE; Type 0: Not a Combination Product
6	NDC:21749-367-68	175 in 1 PACKAGE	02/24/2012
6		479 mL in 1 CANISTER; Type 0: Not a Combination Product

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

Labeler - GOJO Industries, Inc. (004162038)

Name	Address	ID/FEI	Business Operations
Establishment
GOJO Industries, Inc.		036424534	manufacture(21749-367)