DR.S CLEAN HAND SANITIZER- ethyl alcohol gel 
Erf Exhibit Inc

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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Dr.s CLEAN HAND SANITIZER

Drug Facts

Active ingredients

Ethyl Alcohol 70.0%

Purpose

ANTISEPTIC

Uses

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

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 ifirritation or redness develops.

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

Directions

• Wet hands thoroughly with product and allow to dry without wiping.

• For children under 6, use only under adult supervision.

Inactive Ingredients

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

Questions?

310.537.7662 or visit http://www.megaexhibit.com

HAND GEL

Simply KILL 99.9% Germ

Leaves Hands Feeling Soft

ADVANCED

(ethanol) contented 

ERF

12854 E. Florence Ave. Santa Fe Springs, CA 90670

Packaging

untitled

DR.S CLEAN HAND SANITIZER 
ethyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76724-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  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:76724-001-05500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/04/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A05/04/2020
Labeler - Erf Exhibit Inc (099461452)

Revised: 5/2020
Document Id: d9aaca01-7297-4e8b-b1a9-270a6bf515a9
Set id: 77545e56-21dd-4f31-b6dc-9d5a2c014d8a
Version: 1
Effective Time: 20200505
 
Erf Exhibit Inc