PURELL SANITIZING WIPES- benzalkonium chloride swab

PURELL Hand Sanitizing Wipes by

Drug Labeling and Warnings

PURELL Hand Sanitizing Wipes by is a Otc medication manufactured, distributed, or labeled by GOJO Industries, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial

Uses

• Hand sanitizer to help reduce bacteria on the skin

Warnings

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), Decyl Glucoside, Glycerin, Fragrance(Parfum), Methylparaben, Phenoxyethanol, Propylparaben

Questions?

• Call 1-800-321-9647
• www.GOJO.com

Package/Label Principal Display Panel

Purell 

SANITIZING WIPES
Kills 99.99% of most common germs

270 Wet Wipes - 6 in. x 6.75 in. (15.2 cm x 17.1 cm)

INGREDIENTS AND APPEARANCE

PURELL SANITIZING WIPES 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 21749-368
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.0013

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
GLYCERIN (UNII: PDC6A3C0OX)
METHYLPARABEN (UNII: A2I8C7HI9T)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 21749-368-35	35 in 1 CANISTER
2	NDC: 21749-368-10	100 in 1 CANISTER
3	NDC: 21749-368-27	270 in 1 CANISTER
4	NDC: 21749-368-12	1200 in 1 POUCH
5	NDC: 21749-368-15	1500 in 1 POUCH

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

Labeler - GOJO Industries, Inc. (004162038)

Establishment
Name	Address	ID/FEI	Business Operations
GOJO Industries, Inc.		036424534	MANUFACTURE(21749-368)