PURELL SF607 INSTANT HAND SANITIZING- benzalkonium chloride liquid

PURELL SF607 Instant Hand Sanitizing by

Drug Labeling and Warnings

PURELL SF607 Instant Hand 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

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

• Place enough product in your palm to thoroughly cover your hands
• Rub hands together briskly until dry
• Children under 6 years of age should be supervised when using this product.

INACTIVE INGREDIENT

Water (Aqua), Decyl Glucoside, Glycerin, Methylparaben, Phenoxyethanol, Propylparaben

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PURELL SF607 INSTANT HAND SANITIZING 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 21749-607
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
METHYLPARABEN (UNII: A2I8C7HI9T)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 21749-607-31	45 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/03/2011
2	NDC: 21749-607-53	535 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/03/2011
3	NDC: 21749-607-89	1200 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/03/2011

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/03/2011

Labeler - GOJO Industries, Inc. (004162038)

Establishment
Name	Address	ID/FEI	Business Operations
GOJO Industries, Inc.		036424534	manufacture(21749-607)

Establishment
Name	Address	ID/FEI	Business Operations
GOJO Industries, Inc.		088312414	label(21749-607) , pack(21749-607)