Label: MY MEDIC SUPER SANITIZER- ethyl alcohol gel

  • NDC Code(s): 81417-008-01
  • Packager: Sled Distribution, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 15, 2024

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  • Active Ingredients

    Ethyl Alcohol 72%

  • Purpose

    Antiseptic

  • Uses

    • to decrease bacterica on the skin that could cause diease
    • single use
  • Warnings

    For external use only: Hands​

    Flammable: Keep away from fire or flame.

  • WHEN USING

    When using this product

    • Keep out of eyes. ln case of contact with eyes, flush thoroughly with water.
    • Avoid contact with broken skin.
    • Do not inhale or ingest.
  • STOP USE

    Stop use and ask a doctor if

    • irritation and redness develop.
    • Condition persists for more than 72 hours.
  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of 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.
    • For children under 6, use only under adult supervision.
    • Not recommended for infants.
  • Inactive ingredients

    Aloe Barbadensis Leaf Juice, Fragrance, Glycerin, Maltodextrin, Propylene Glycol, Triethanolamine Acrylates/C10-30 Alkyl Acrylate Cross Polymer, Water.

  • PRINCIPAL DISPLAY PANEL

    image of pouch label

  • INGREDIENTS AND APPEARANCE
    MY MEDIC SUPER SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81417-008
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL72 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81417-008-012 g in 1 POUCH; Type 0: Not a Combination Product08/29/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00508/29/2022
    Labeler - Sled Distribution, LLC (079772888)
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