Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

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.

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.

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.

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

Glacier Ultra Blue Antibacterial Foaming Skin Cleanser

Purpose

Antibacterial

Glacier Blue Antibacterial Foaming Skin Cleanser

KEEP OUT OF REACH OF CHILDREN

Glacier Blue Antibacterial Foaming Skin Cleanser

759-29 bag-1000ml 759-29

GLACIER BLUE ANTIBACTERIAL FOAMING SKIN CLEANSER
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:62428-759
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
COCAMINE OXIDE (UNII: QWA2IZI6FI)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PEG-4 RAPESEEDAMIDE (UNII: 89575CN928)
COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
EDETATE SODIUM (UNII: MP1J8420LU)
ALCOHOL (UNII: 3K9958V90M)
BENZYL ACETATE (UNII: 0ECG3V79ZJ)
SODIUM GLYCOLATE (UNII: B75E535IMI)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
TRISODIUM NITRILOTRIACETATE (UNII: E3C8R2M0XD)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
N-ALKYL DIMETHYL BENZYL AMMONIUM CHLORIDE (C12-C18) (UNII: 9U1Q4T4ZYS)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
2,4-DIMETHYL-3-CYCLOHEXENE CARBOXALDEHYDE (UNII: 452GFV2AFS)
METHYL DIHYDROJASMONATE (SYNTHETIC) (UNII: 3GW44CIE3Y)
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)
MAGNESIUM NITRATE (UNII: 77CBG3UN78)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
GERANIOL (UNII: L837108USY)
LIME OIL (UNII: UZH29XGA8G)
2-METHYLUNDECANAL (UNII: S94QNS2VY5)
.BETA.-CITRONELLOL, (+/-)- (UNII: 565OK72VNF)
ALLYL CYCLOHEXANEPROPIONATE (UNII: H4W9H3L241)
GERANYL ACETATE (UNII: 3W81YG7P9R)
CITRONELLYL ACETATE (UNII: IZ420RT3OY)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
CITRAL (UNII: T7EU0O9VPP)
FORMALDEHYDE (UNII: 1HG84L3525)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:62428-759-29	1000 mL in 1 BAG; Type 0: Not a Combination Product	11/12/2012
2	NDC:62428-759-03	750 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	11/12/2012

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	11/12/2012

Labeler - Lawson Products, Inc (005438890)

Registrant - Betco Corporation, Ltd (024492831)

Name	Address	ID/FEI	Business Operations
Establishment
Betco Corporation, Ltd		024492831	manufacture(62428-759) , label(62428-759)