ALPET Q E2- benzalkonium chloride liquid
Best Sanitizers, Inc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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ALPET Q E2 Sanitizing Foam Soap

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

Alpet Q E2 Sanitizing Foam Soap

NSF

Principal Display Panel

ALPET Q E2
benzalkonium chloride liquid

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

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

Ingredient Name	Strength
Inactive Ingredients
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)

#	Item Code	Package Description	Marketing Start Date
Packaging
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 Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	07/15/2009

Labeler - Best Sanitizers, Inc (957473614)

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