Label: ADRIANA 12OZ HAND SANITIZER- alcohol gel

  • 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 January 31, 2018

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  • Active ingredient

    Ethyl Alcohol 62.0%

  • Purpose

    Antimicrobial

  • Uses

    hand sanitizer to help reduce bacteria on the skin.

  • Warnings

    For external use only.

  • WARNINGS

    Flammable. Keep away from heat and flame.

  • When using this product

    avoid contact with face, eyes, and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

  • Stop use and ask a doctor if

    irritation or redness develops.

  • Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center.

  • Directions

    • wet hands thoroughly with product and rub into skin until dry.
    • Children under 6 years of age should be supervised by an adult when using this product.
  • Inactive ingredients

    Water (Aqua), Aloe Barbadensis Leaf Juice, Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate (Vitamin E), Triethanolamine

  • SPL UNCLASSIFIED SECTION

    *Kills 99.9% of many common germs.

    Imported by: O.S.T.L. Inc

    Made in P.R.C.

    Distributed by: VERNON SALES. INC

    www.ostltrade.com

  • Drug Facts

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    ADRIANA 12OZ HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69950-023
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69950-023-01355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/31/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E01/31/2018
    Labeler - OSTL, INC. (020117798)
    Registrant - OSTL, INC. (020117798)
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