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Hand Sanitizer by CMC Group Inc.

Dosage form: gel
Ingredients: ALCOHOL 0.62g in 1g
Labeler: CMC Group Inc.
NDC Code: 49687-0015

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.

Hand Sanitizer

Drug Facts

Active ingredient

Ethyl alcohol 62%

Purpose

Antiseptic

Uses
  • For handwashing to decrease bacteria on the skin
  • Recommended for repeated use.

Warnings

Flammable, keep away from fire or flame

For external use only.

Do not use
  • in the eyes.

Stop use and ask a doctor if
  • irritation and redness develop
  • condition persists for more than 72 hours

Keep out of reach 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.

Other information

Store at 15° to 25°C (59° to 77°F)

Inactive ingredients

Carbomer, propylene glycol, purified water, titanium dioxide

Package Labeling

HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49687-0015
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL0.62 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
CARBOXYPOLYMETHYLENE 
PROPYLENE GLYCOL 
WATER 
TITANIUM DIOXIDE 
Packaging
#Item CodePackage Description
1NDC:49687-0015-06 PACKAGE in 1 BOX
10.9 g in 1 PACKAGE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E08/08/2016
Labeler - CMC Group Inc. (005583328)

 
CMC Group Inc.

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Medically reviewed on Aug 10, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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