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Antimicrobial Alcohol Hand

Dosage form: patch
Ingredients: ALCOHOL 65.9g in 100g
Labeler: Geri-Gentle Corporation
NDC Code: 69771-002

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.

Antimicrobial Alcohol Gel Hand wipe

Drug Facts

Active ingredient

Alcohol 65.9% by volume



  • Antiseptic 
  • For handwashing to decrease bacteria on the skin, assisting ill persons, and before contact with a person under medical care or treatment
  • Apply topically to the skin to help prevent cross-contamination
  • Recommended for repeated use 
  • Dries in seconds

  • Flammable, keep away from fire or flame
  • For external use only

Do not use
  • in or make contact with the eyes
  • Discontinue use if irritation and redness develop. If condition persists for more than 72 hours consult a physician 

Keep this our of reach of children
  • unless under adult supervision 
  • If swallowed, get medical help or contact a Poison Center immediately

  • To start feed: Remove cover and discard seal from container. From center of toweled roll, pull up wipe corner, tear off fist wipe for use. Twist next wipe into a point and thread through the hole in the container cover. Pull through about one inch. Replace cover. Pull out wipes as needed and snap off at 90° angle. Keep cap closed to prevent moisture loss
  • Wipe hands , fingers, interdigital areas and wrists thoroughly with towelette. Be sure to utilize the entire wipe surface. Allow to dry
  • If hands are visibly soiled or contaminated, use first wipe to clean hands, then discard wipe, Sanitize with a second wipe
  • Discard after single use

Other information

Lot No. and Expiration Date can be found on canister

Inactive ingredients

Water, Propylene Glycol, Glycerin, Carbomer, Triethanolamine, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Tetrasodium EDTA

Package Labeling:

alcohol patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69771-002
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
#Item CodePackage Description
1NDC:69771-002-00135 PATCH in 1 CANISTER
16.59 g in 1 PATCH
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E04/05/2017
Labeler - Geri-Gentle Corporation (361663839)

Revised: 01/2018
Geri-Gentle Corporation

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.