GLACIER BLUE ANTIBACTERIAL FOAMING HAND WASH- benzalkonium chloride soap

Glacier Blue Antibacterial Foaming Hand Wash by

Drug Labeling and Warnings

Glacier Blue Antibacterial Foaming Hand Wash by is a Otc medication manufactured, distributed, or labeled by Lawson Product, Inc, Betco Corporation, Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Glacier Blue Antibacterial Foaming Hand Wash Active Ingredient

Benzalkonium Chloride 0.13%

Glacier Blue Antibacterial Foaming Hand Wash Purpose

Antibacterial

Glacier Blue Antibacterial Foaming Hand Wash Warnings

• For external use only. Do not ingest.
• Avoid contact with eyes. If contact occurs, rinse thoroughly with water.
• Stop use and ask a doctor if irritation and redness develop.
• 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.

Glacier Blue Antibacterial Foaming Hand Wash Directions

• ?Read the entire label before using this product.
• ?Dispense 2 pumps of product onto palm of hand and scrub thoroughly over all surfaces of both hands.
• Rinse with clean water.

Glacier Blue Antibacterial Foaming Hand Wash Inactive Ingredients

Water, Phenoxyethanol, Cocamine Oxide, Propylene Glycol, Decyl Glucoside, PEG-4 Rapeseedamide, Cocamidopropyl Hydroxysultaine, Glycerin, Fragrance, Sodium Chloride, Tetrasodium EDTA, Citric Acid, Ethanol, Iodopropynyl Butylcarbamate, Benzyl Acetate, Sodium Glycolate, Sodium Hydroxide, Trisodium Nitrilotriacetate, Diethyl Phthalate, FD&C Blue #1.

Glacier Blue Antibacterial Foaming Hand Wash Questions

Questions? 888-GO BETCO (888-462-3826)

Glacier Blue Antibacterial Foaming Hand Wash Purpose

Purpose

Antibacterial

Glacier Blue Antibacterial Foaming Hand Wash Keep out of Reach of Childen

KEEP OUT OF REACH OF CHILDREN

Glacier Blue Antibacterial Foaming Hand Wash Package Label

75929_Drummond_GlacierBlueAntibacterial

INGREDIENTS AND APPEARANCE

GLACIER BLUE ANTIBACTERIAL FOAMING HAND WASH 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62428-711
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   in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
COCAMINE OXIDE (UNII: QWA2IZI6FI)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
PEG-4 RAPESEEDAMIDE (UNII: 89575CN928)
COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
EDETATE SODIUM (UNII: MP1J8420LU)
CITRIC ACID ACETATE (UNII: DSO12WL7AU)
ALCOHOL (UNII: 3K9958V90M)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
BENZYL ACETATE (UNII: 0ECG3V79ZJ)
SODIUM GLYCOLATE (UNII: B75E535IMI)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
TRISODIUM NITRILOTRIACETATE (UNII: E3C8R2M0XD)
DIETHYL PHTHALATE (UNII: UF064M00AF)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62428-711-29	1000 mL in 1 BAG; Type 0: Not a Combination Product	04/01/2019
2	NDC: 62428-711-57	550 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/01/2019
3	NDC: 62428-711-03	750 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/01/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/01/2019

Labeler - Lawson Product, Inc (005438890)

Registrant - Betco Corporation, Ltd (024492831)

Establishment
Name	Address	ID/FEI	Business Operations
Betco Corporation, Ltd		024492831	label(62428-711) , manufacture(62428-711)