ESTHETE HAND SANITIZER- ethyl alcohol gel

ESTHETE HAND SANITIZER by

Drug Labeling and Warnings

ESTHETE HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by EQMAXON Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ethyl Alcohol 70.0%

INACTIVE INGREDIENTS

PURIFIED WATER, ALOE EXTRACT, GLYCERIN, SODIUM HYALURONATE, CARBOMER, BUTYLENE GLYCOL, AMINOMETHYL PROPANOL, FRAGRANCE

PURPOSE

ANTISEPTIC

WARNINGS

▪ FOR EXTERNAL USE ONLY ▪ FLAMMABLE, KEEP AWAY FROM FIRE AND FLAME

When using this product
▪Keep out of eyes. In case of contact with eyes, flush thoroughly with water. ▪ Avoid contact with broken skin ▪ Do not inhale or ingest.

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

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a Poison Control Center right away

Uses

HAND SANITIZER TO HELP REDUCE BACTERIA ON THE SKIN

Directions

▪ DISPENSE ONE TO TWO PUMPS OF SANITIZER ONTO HANDS AND RUB THOROUGHLY UNTIL DRY.

▪ USE AS NEEDED ▪ FOR CHILDREN UNDER 6, USE WITH ADULT SUPERVISION

▪ NOT RECOMMENDED FOR INFANTS

Other Information

▪ Store below 110 °F(43°C)

▪ May discolor some fabrics

▪ Harmful to wood finishes and plastics

Questions or Comments?

Email : gajoany@gmail.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ESTHETE HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55526-0014
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	350 mL  in 500 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
ALOE (UNII: V5VD430YW9)
Glycerin (UNII: PDC6A3C0OX)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
Butylene Glycol (UNII: 3XUS85K0RA)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55526-0014-1	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/01/2020

Labeler - EQMAXON Corp (557821534)

Registrant - EQMAXON Corp (557821534)

Establishment
Name	Address	ID/FEI	Business Operations
EQMAXON Corp		557821534	manufacture(55526-0014)