Label: ANTIMICROBIAL ALCOHOL HAND- alcohol patch

  • NDC Code(s): 69771-002-00
  • Packager: Geri-Gentle Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 10, 2023

If you are a consumer or patient please visit this version.

  • Drug Facts

  • Active ingredient

    Alcohol 65.9% by volume

    Purpose

    Antiseptic  

  • Uses

    • 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
  • Warnings

    • 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
  • Directions

    • 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

  • SPL UNCLASSIFIED SECTION

  • Package Labeling:

    Label 2

  • INGREDIENTS AND APPEARANCE
    ANTIMICROBIAL ALCOHOL HAND 
    alcohol patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69771-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL65.9 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69771-002-00135 in 1 CANISTER04/05/2017
    16.59 g in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)04/05/2017
    Labeler - Geri-Gentle Corporation (080367686)