Drug Facts 59900-214

Active ingredient

Benzalkonium Chloride 0.12%

Purpose

Antiseptic Hand Cleanser

Uses

handwash to help reduce bacteria that potentially can cause disease

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 productdo not use in or near eyes

Stop use and ask a doctor ifirritation or redness develop.

Keep out of reach of children.

If swallowed, seek medical attention or contact a Poison Control Center immediately.

Directions

wet hands and wrists with clean, running water

apply appropriate amount of product

lather and scrub hands, fingers, fingernails, cuticles and wrists for at least 20 seconds

rinse thoroughly with running water

dry hands completely (incomplete drying may result in chapped skin)

Other information

store in a cool, dry place below 104 oF (40 oC)

Inactive ingredients

Water, cocamidopropyl betaine, glycerine, polyethylene-polypropylene glycol, benzyl alcohol, phenoxyethanol, tetra sodium EDTA, dehydroacetic acid, sodium hydroxide, citric acid

Questions?

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

Maximize the Clean

BEST SANITIZERS INC.

ALPET Q E2

Sanitizing Foam Soap

For Food Industry

Professionals

Tough on germs,

but gentle on hands...

even when frequent use!

Fragrance and dye free

NSF certified E2 classification

Kosher, Pareve and Halal certified

Rich, thick foam

0.12% BAC

Benzalkonium Chloride

formula

BEST

SANITIZERS

INC.

NSF

Nonfood Compounds

Program Listed (E2)

Registration Number 143188

Net Contents:

container label

ALPET QE2 SANITIZING FOAM
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:59900-214
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 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
GLYCERIN (UNII: PDC6A3C0OX)
POLOXAMER 124 (UNII: 1S66E28KXA)
BENZYL ALCOHOL (UNII: LKG8494WBH)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
EDETATE SODIUM (UNII: MP1J8420LU)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:59900-214-01	946352 mL in 1 TANK; Type 0: Not a Combination Product	05/03/2019
2	NDC:59900-214-02	208197 mL in 1 DRUM; Type 0: Not a Combination Product	05/03/2019
3	NDC:59900-214-03	3785 mL in 1 JUG; Type 0: Not a Combination Product	05/03/2019
4	NDC:59900-214-05	1250 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/03/2019
5	NDC:59900-214-08	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/03/2019
6	NDC:59900-214-10	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/03/2019

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/03/2019

Labeler - Best Sanitizers, Inc. (957473614)

Name	Address	ID/FEI	Business Operations
Establishment
Best Sanitizers, Inc.		627278224	manufacture(59900-214)