DR.S CLEAN HAND- 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

Active ingredients: Ethyl Alcohol 70.0%

INACTIVE INGREDIENT

Inactive ingredients:

Purified Water, Aloe Extract, Glycerin, Sodium Hyaluronate, Carbomer, Butylene Glycol, Triethanolamine, Flavor

PURPOSE

Purpose: ANTISEPTIC

WARNINGS

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

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

Directions

Directions:

Wet hands thoroughly with product and allow to dry without wiping

For children under 6, use only under adult supervision.

PACKAGE LABEL - Dr.'s Clean Hand Gel 60mL

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PACKAGE LABEL - Dr.'s Clean Hand Gel 500mL

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DR.S CLEAN HAND 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55526-0010
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 g  in 100 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:55526-0010-160 mL in 1 BOTTLE; Type 0: Not a Combination Product03/01/2020
2NDC:55526-0010-2500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E03/01/2020
Labeler - EQMAXON Corp (557821534)
Registrant - EQMAXON Corp (557821534)
Establishment
NameAddressID/FEIBusiness Operations
EQMAXON Corp557821534manufacture(55526-0010)

Revised: 4/2020
Document Id: 5ececc12-b893-4c23-ae05-9aeac28286ca
Set id: fad65262-320f-4348-8932-677c58853991
Version: 1
Effective Time: 20200407
 
EQMAXON Corp