ALPET Q E2- benzalkonium chloride liquid

Alpet Q E2 by

Drug Labeling and Warnings

Alpet Q E2 by is a Otc medication manufactured, distributed, or labeled by Best Sanitizers, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.12%

Purpose

Antiseptic Hand Cleanser

Uses

• Hanwash to help reduce bacteria that potentially can cause diseases
• Helps to prevent cross contamination by hand contact
• Helps to prevent drying of the skin
• Recommended for repeated use

Warnings

• For external use only

When Using this product

• Do not use in or near eyes

Keep out of reach of children

In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

Directions

• Wet hands and forearms
• Apply an application to hands and forearms
• Scrub thoroughly for at least 30 seconds (include the fingernails and the cuticles)
• Rinse

Other information

Store in a cool dry place below 104° F

Inactive ingredients

water, glycerine, cocoamidopropy betaine, polyethylene-polypropylene glycol, benzyl alcohol, phenoxyethanol, tetra sodium EDTA, dehydroacetic acid

Questions?

Contact Best Sanitizers Mon-Fri 9am-4pm PST at 888-225-3267

PRINCIPAL DISPLAY PANEL

Alpet Q E2 Sanitizing Foam Soap

NSF

INGREDIENTS AND APPEARANCE

ALPET Q E2 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59900-130
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.2 g  in 1000 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
BENZYL ALCOHOL (UNII: LKG8494WBH)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
EDETIC ACID (UNII: 9G34HU7RV0)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59900-130-01	1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/15/2009
2	NDC: 59900-130-02	3785.41 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/15/2009
3	NDC: 59900-130-03	208198 mL in 1 DRUM; Type 0: Not a Combination Product	07/15/2009
4	NDC: 59900-130-04	946353 mL in 1 DRUM; Type 0: Not a Combination Product	07/15/2009

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/15/2009

Labeler - Best Sanitizers, Inc (957473614)

Establishment
Name	Address	ID/FEI	Business Operations
Best Sanitizers, Inc		627278224	manufacture(59900-130)