ALPET E2 SANITIZING FOAM- chloroxylenol liquid

ALPET E2 Sanitizing Foam by

Drug Labeling and Warnings

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

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient

Chloroxylenol (1.5% w/w)

PURPOSE

Purpose

Antiseptic Hand Cleanser

INDICATIONS & USAGE

Uses

• handwash to help reduce bacteria that potentially can cause disease

• helps prevent cross-contamination by hand contact

• helps to prevent drying of the skin

• recommended for repeated use
  

WARNINGS

Warnings

For external use only

When using this product do not use in or near eyes

Stop use and ask a doctor if irritation or redness develop.

Keep out of reach of children.

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

DOSAGE & ADMINISTRATION

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 chapping skin)
  

STORAGE AND HANDLING

Other information

store in a cool, dry place below 104o F (40o C)

INACTIVE INGREDIENT

Inactive ingredients

Water, sodium laureth sulfate, isopropyl alcohol, phenoxyethanol, glycerine, TetraSodium EDTA, citric acid, sodium hydroxide

QUESTIONS

Questions?

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

PRINCIPAL DISPLAY PANEL

Maximize the Clean

BEST SANITIZERS INC.

ALPET E2

Sanitizing

Foam

Soap

For Food Industry

Professionals

Tough on germs,

but gentle on hands!

Fragrance and dye free

NSF certified E2 classification

Kosher certified and Pareve

Rich, thick foam

1.5% PCMX

formula

BEST

SANITIZERS

INC.

NSF

Nonfood Compounds

Program Listed (E2)

Registration Number 140904

Net Contents:

INGREDIENTS AND APPEARANCE

ALPET E2 SANITIZING FOAM 
chloroxylenol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59900-128
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	15 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
GLYCERIN (UNII: PDC6A3C0OX)
EDETATE SODIUM (UNII: MP1J8420LU)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59900-128-01	946352 mL in 1 TANK; Type 0: Not a Combination Product	05/14/2019
2	NDC: 59900-128-02	208197 mL in 1 DRUM; Type 0: Not a Combination Product	05/14/2019
3	NDC: 59900-128-03	3785 mL in 1 JUG; Type 0: Not a Combination Product	05/14/2019
4	NDC: 59900-128-05	1250 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/14/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/14/2019

Labeler - Best Sanitizers, Inc. (957473614)

Establishment
Name	Address	ID/FEI	Business Operations
Best Sanitizers, Inc.		627278224	manufacture(59900-128)