Label: HAND SANITIZER- alcohol cloth

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 17, 2023

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  • Active Ingredient(s)

    Ethyl Alcohol 70% v/v. Purpose: Antiseptic Wipe

  • Purpose

    Antiseptic Wipe

  • Use

    For hand washing to decrease bacteria on the skin. Recommended for repeated use.

  • Warnings

    For external use only. Flammable. Keep away from heat or flame. Do not use in the eyes.

  • WHEN USING

    When using this product avoid contact with eyes. In case of eye contact, rinse with water to remove.



    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

  • STOP USE

    Stop use and ask a doctor if irritation and redness develop.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

  • Directions

    • To start feed: Remove cover and discard seal from container, from center fo toweled roll, pull up wipe corner, tear off first 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 a 90 degree 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

    • Do not store above 110 degrees F
  • Inactive ingredients

    Aloe Barbadensis Leaf Juice, Cabormer, Diazolidinyl Urea, Glycerin, Methylparaben, Polysorbate 20, Propylene Glycol, Propylparaben, Tocopheryl Acetate, Triethanolamine, Water

  • Package Label - Principal Display Panel

    Label

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70000-0579
    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
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    WATER (UNII: 059QF0KO0R)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70000-0579-1135 mL in 1 CANISTER; Type 0: Not a Combination Product09/20/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00309/20/2021
    Labeler - Cardinal Health (063997360)
    Registrant - Phoenix Healthcare Solutions, LLC (079146847)
    Establishment
    NameAddressID/FEIBusiness Operations
    Phoenix Innovative Healthcare650743854manufacture(70000-0579)
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