Label: MY MEDIC HAND SANITIZER WITH ALOE VERA- ethyl alcohol liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

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 Label Information

Updated April 27, 2021

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

  • Active Ingredient

    Ethyl Alcohol     72%

    Purpose

    Antiseptic

  • USE

    • To decrease bacterica on the skin that could cause diease. 
    • Signle use
  • Warning

    • For external use only: hands
    • Flammable: keep away from fire or flame.

    When using this product

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

    Stop use and ask a doctor,

    • Irritaion and redness develop.
    • Condition persists for more than 72 hours.

    Other Information:

    • Do not store above 110℉.
    • May discolor some fabrics.
    • Harmul to wood finishes and plastics.

    ●If swallowed, get medical help or contact a Poison Contrl 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

    label image

  • INGREDIENTS AND APPEARANCE
    MY MEDIC HAND SANITIZER WITH ALOE VERA 
    ethyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81417-002
    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
    water (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81417-002-012 g in 1 PACKAGE; Type 0: Not a Combination Product04/27/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/27/2021
    Labeler - Sled Distribution, LLC (079772888)
    Establishment
    NameAddressID/FEIBusiness Operations
    Sled Distribution, LLC079772888manufacture(81417-002)