PURELL PERSONAL PACK SANITIZING- alcohol swab

Purell Personal Pack Sanitizing by

Drug Labeling and Warnings

Purell Personal Pack Sanitizing 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

Antiseptic Cleanser

Uses

• Hand sanitizer to help reduce bacteria on the skin

Warnings

Flammable. Keep away from fire or flame and sources of heat.

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 redness develops

Keep Out of Reach of Children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• This product should be used as part of the daily cleansing routine.
• Wipe hands; allow to dry. Discard.

Other information

• Do not store above 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

Questions?

1-800-321-9647

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PURELL PERSONAL PACK SANITIZING 
alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 21749-366
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)
CORN OIL (UNII: 8470G57WFM)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 21749-366-95	135 mL in 1 POUCH; Type 0: Not a Combination Product	03/14/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/14/2012	01/01/2021

Labeler - GOJO Industries, Inc. (004162038)

Establishment
Name	Address	ID/FEI	Business Operations
GOJO Industries, Inc.		036424534	MANUFACTURE(21749-366)