DR.S CLEAN ADVANCED HAND- 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, Triethanolamine, Flavoring

PURPOSE

ANTISEPTIC

WARNINGS

Flammable. Keep away from fire and flames. For external use only.


When using this product • Do not get into eyes. • If contact occurs, rinse eyes thoroughly with water.


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

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Uses

for hand-washing to decrease bacteria on the skin, only when water is not available

Directions

Wet hands thoroughly with product and allow to dry without wiping

For children under 6, use only under adult supervision.

Questions

Questions?

+82-31-429-8582 or visit http://www.eqmaxon.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottle

DR.S CLEAN ADVANCED HAND 
ethyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55526-0016
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL42 mL  in 60 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)  
TROLAMINE (UNII: 9O3K93S3TK)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55526-0016-160 mL in 1 BOTTLE; Type 0: Not a Combination Product07/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E07/01/2020
Labeler - EQMAXON Corp (557821534)
Registrant - EQMAXON Corp (557821534)
Establishment
NameAddressID/FEIBusiness Operations
EQMAXON Corp557821534manufacture(55526-0016)

Revised: 7/2020
Document Id: 15606713-7cec-4b6c-8676-a23fbca0f597
Set id: d23af803-95c8-47f3-a0ee-ecbf6c328eae
Version: 1
Effective Time: 20200727
 
EQMAXON Corp