ESTHETE HAND SANITIZER- ethyl alcohol gel 
EQMAXON Corp

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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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

Image of bottle

ESTHETE HAND SANITIZER 
ethyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55526-0014
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL350 mL  in 500 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55526-0014-1500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E05/01/2020
Labeler - EQMAXON Corp (557821534)
Registrant - EQMAXON Corp (557821534)
Establishment
NameAddressID/FEIBusiness Operations
EQMAXON Corp557821534manufacture(55526-0014)

Revised: 5/2020
Document Id: 90b0b110-cb40-41d8-bb9b-cf6f9273dc98
Set id: 52ae9023-e397-4954-9b53-c69936c9b216
Version: 1
Effective Time: 20200530
 
EQMAXON Corp