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Antimicrobial Hand Sanitizer by Hanover Pen Corp dba HPC Global

Dosage form: gel
Ingredients: Alcohol 19.66mL in 29.57mL
Labeler: Hanover Pen Corp dba HPC Global
NDC Code: 51811-362

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.

Drug Facts

Active Ingredient

Ethyl Alcohol 66.5 percent




For handwashing to decrease bacteria on skin.

Recommended for repeated use.

For external use only.

Flammable, keep away from fire or flame.

Do not use in the eyes, if this happens rinse thoroughly with water.

Stop use and ask a doctor if irritation of redness develops and persists for more than 72 hours.

Keep out of reach of children.

If ingested get medical help or contact a Poison Control Center right away.


wet hands throughly with product allow to dry without wiping

children under six should be supervised while using this product.

Inactive Ingredients

aloe vera, carbomer, fragrance, purified water, triethanolamine

Drug Facts

alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51811-362(NDC:61010-111)
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Alcohol (Alcohol) Alcohol19.66 mL  in 29.57 mL
Inactive Ingredients
Ingredient NameStrength
#Item CodePackage Description
1NDC:51811-362-2129.57 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E09/13/2010
Labeler - Hanover Pen Corp dba HPC Global (003022670)
Hanover Pen Corp dba HPC Global003022670repack, label

Hanover Pen Corp dba HPC Global

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Medically reviewed on Sep 13, 2018

Further information

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