ALPET E3 HAND SANITIZER FOAM- alcohol liquid

ALPET E3 HAND SANITIZER FOAM by

Drug Labeling and Warnings

ALPET E3 HAND SANITIZER 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

Alcohol 62.0%

PURPOSE

Purpose

Hand Sanitizer

INDICATIONS & USAGE

Uses

• sanitizes hands to help reduce bacteria that potentially can cause disease

• helps to prevent cross-contamination

• recommended for repeated use

• helps prevent drying of skin
  

WARNINGS

Warnings

• For external use only

• Flammable, keep away from fire or flame
  

When using this product

• do not use in or near eyes

• use in a well-ventilated area
  

Stop use and consult 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

• receive an adequate amount of foam into palm of hand

• rub thoroughly over all surfaces of both hands

• rub hands together until dry
  

STORAGE AND HANDLING

Other Information

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

INACTIVE INGREDIENT

Inactive Ingredients

Water, DEA-C8-18 perfluoroalkylethyl phosphate, glycereth-2 cocoate, denatonium benzoate, tert-butyl alcohol

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 E3

Hand Sanitizer Foam

For Food Industry

Professionals

Meets all FDA (GRAS) and

USDA requirements for

food handling

Enhanced with moisturizers

to keep skin soft and healthy

NSF certified E3 classification

Kosher certified and Pareve

Kills

99.999%

of tested pathogens

in 15 seconds

BEST

SANITIZERS

INC.

NSF

Nonfood Compounds

Program Listed E3

Registration Number143167

Net Contents:

INGREDIENTS AND APPEARANCE

ALPET E3 HAND SANITIZER FOAM 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59900-125
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DIETHANOLAMINE BIS(C8-C18 PERFLUOROALKYLETHYL)PHOSPHATE (UNII: 4J55VM509S)
GLYCERETH-2 COCOATE (UNII: JWM00VS7HC)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59900-125-02	208197 mL in 1 DRUM; Type 0: Not a Combination Product	05/01/2019
2	NDC: 59900-125-05	1250 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2019
3	NDC: 59900-125-08	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/01/2019

Labeler - Best Sanitizers, Inc. (957473614)

Establishment
Name	Address	ID/FEI	Business Operations
Best Sanitizers, Inc.		627278224	manufacture(59900-125)