ALCOHOL FREE FOAMING HAND SANITIZER- benzalkonium chloride soap

Alcohol Free Foaming Hand Sanitizer by

Drug Labeling and Warnings

Alcohol Free Foaming Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Betco Corporation, Ltd., Betco corporation, Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Alcohol Free Foaming Hand Sanitizer

​Active Ingredient

Benzalkonium Chloride 0.13%

Alcohol Free Foaming Hand Sanitizer

Uses

• Hand sanitizer to remove microorganisms on the skin.
• Use this product when soap and water are not available.

Alcohol Free Foaming Hand Sanitizer

Warnings

• For external use only.
• Avoid contact with eyes. If contact occurs, rinse thoroughly with water.
• Discontinue use is irritation or redness develops.
• If irritation persists for more than 72 hours, consult a physician.
• KEEP OUT OF REACH OF CHILDREN.
• If swallowed, get medical help or contact a Poison Control Center right away.

Alcohol Free Foaming Hand Sanitizer

Directions

• ​Read the entire label before using this product.
• ​Dispense 2 pumps of product onto palm of hand and rub thoroughly over all surfaces of both hands until dry.

Alcohol Free Foaming Hand Sanitizer

Inactive Ingredients

Deionized ​Water, Sodium PCA, PEG/PPG-8/3 Laurate, Dimethicone,  PEG-3 Cocamide, Fragrance, Methyl Chloro Isothiazolinone, Methyl Isothiazolinone,  D&C Green #5.

Alcohol Free Foaming Hand Sanitizer

Questions or Comments?Phone: (800) 777-9343

MDS information:​(800) 891-4965

Alcohol Free Foaming Hand Sanitizer

Purpose

Antiseptic

Alcohol Free Foaming Hand Sanitizer

KEEP OUT OF REACH OF CHILDREN

Alcohol Free Foaming Hand Sanitizer

INGREDIENTS AND APPEARANCE

ALCOHOL FREE FOAMING HAND SANITIZER 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65601-700
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
DIMETHICONE (UNII: 92RU3N3Y1O)
PEG-3 COCAMINE (UNII: KTM00873VC)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
2-METHYL-4-ISOTHIAZOLIN-3-ONE HYDROCHLORIDE (UNII: 3G9PNZ5P41)
D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)

Product Characteristics
Color	blue	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65601-700-53	50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/01/2016
2	NDC: 65601-700-29	1000 mL in 1 BAG; Type 0: Not a Combination Product	01/01/2016
3	NDC: 65601-700-04	3780 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/01/2016
4	NDC: 65601-700-57	550 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/01/2016
5	NDC: 65601-700-55	207900 mL in 1 DRUM; Type 0: Not a Combination Product	01/01/2016
6	NDC: 65601-700-03	750 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	09/15/2016
7	NDC: 65601-700-05	1250 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	09/15/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	11/12/2012

Labeler - Betco Corporation, Ltd. (024492831)

Registrant - Betco corporation, Ltd. (024492831)

Establishment
Name	Address	ID/FEI	Business Operations
Betco Corporation, Ltd.		024492831	manufacture(65601-700) , pack(65601-700) , label(65601-700)