PURELL COTTONY SOFT- alcohol swab

PURELL Cottony Soft by

Drug Labeling and Warnings

PURELL Cottony Soft 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

• Tear open, unfold and apply to hands
• Children under 6 years of age should be supervised when using PURELL

Other information

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

Questions?

• Call 1-800-321-9647 Monday through Friday 8:30 AM to 5:00 PM
• www.PURELL.com

Inactive ingredients

Water (Aqua), Isopropyl Alcohol, Glycerin, Acetamidopropyl Trimonium Chloride, Aloe Barbadensis Leaf Juice, C12-15 Alkyl Benzoate, Cocamidopropyl PG-Dimonium Chloride Phosphate, Isopropyl Myristate, Propylene Glycol, Retinyl Palmitate, Tocopheryl Acetate, Zea Mays (Corn) Oil, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance (Parfum), Methylparaben

Package/Label Principal Display Panel

PURELL
Cottony Soft
SANITIZING WIPE

Kills 99.99% of germs

Clean, Sanitize &
Moisturize Hands On The Go

Not for Retail Sale

ONE WIPE 7 in. x 5 in. (18 cm x 13 cm)

Carton Label

INGREDIENTS AND APPEARANCE

PURELL COTTONY SOFT 
alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 21749-364
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)
BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
CORN OIL (UNII: 8470G57WFM)
METHYLPARABEN (UNII: A2I8C7HI9T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 21749-364-76	120 in 1 CARTON
1		4 mL in 1 POUCH

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(21749-364)