PURELL HAND SANITIZING WIPES CLEAN REFRESHING SCENT- benzalkonium chloride wipe liquid

PURELL Hand Sanitizing Wipes Clean Refreshing Scent by

Drug Labeling and Warnings

PURELL Hand Sanitizing Wipes Clean Refreshing Scent 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%

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial

Use

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PURELL HAND SANITIZING WIPES CLEAN REFRESHING SCENT 
benzalkonium chloride wipe liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 21749-359
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.00013

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: 21749-359-15	15 in 1 PACKAGE; Type 0: Not a Combination Product	08/01/2014
2	NDC: 21749-359-20	20 in 1 PACKAGE; Type 0: Not a Combination Product	08/01/2014
3	NDC: 21749-359-40	40 in 1 PACKAGE; Type 0: Not a Combination Product	08/01/2014
4	NDC: 21749-359-70	70 in 1 PACKAGE; Type 0: Not a Combination Product	08/01/2014
5	NDC: 21749-359-10	10 in 1 PACKAGE; Type 0: Not a Combination Product	08/01/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/01/2014

Labeler - GOJO Industries, Inc. (004162038)