PURELL ALCOHOL FORMULATION- alcohol swab

Purell Alcohol Formulation by

Drug Labeling and Warnings

Purell Alcohol Formulation by is a Otc medication manufactured, distributed, or labeled by GOJO Industries, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PURELL ALCOHOL FORMULATION 
alcohol swab

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

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.62 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 21749-367-76	4 mL in 1 POUCH; Type 0: Not a Combination Product	02/24/2012
2	NDC: 21749-367-24	96 mL in 1 PACKAGE; Type 0: Not a Combination Product	02/24/2012
3	NDC: 21749-367-36	144 mL in 1 PACKAGE; Type 0: Not a Combination Product	02/24/2012
4	NDC: 21749-367-63	315 mL in 1 CANISTER; Type 0: Not a Combination Product	02/24/2012
5	NDC: 21749-367-94	540 mL in 1 PACKAGE; Type 0: Not a Combination Product	02/24/2012
6	NDC: 21749-367-68	700 mL in 1 CANISTER; Type 0: Not a Combination Product	02/24/2012

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	Business Operations
GOJO Industries, Inc.		036424534	manufacture(21749-367)