Label: MISSY KAY PREMIUM 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 April 13, 2020

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  • ACTIVE INGREDIENT

    Active ingredients: 62.0%(w/w)

  • INACTIVE INGREDIENT

    Inactive ingredients:

    Water, Carbomer, Triethanolamine, Polyoxyethylene Hydrogenated Castor Oil, Lavandula Angustifolia (Lavender) Oil, Methylparaben, Butylene Glycol, Hexylene Glycol, Strawberry Extract, Sophora Extract, Mulberry Root Extract, Glycyrrhiza Extract, Grapefruit Extract, Green Tea Extract

  • PURPOSE

    Purpose: ANTISEPTIC

  • WARNINGS

    Warnings:

    ■ Flammable. Keep away from fire or flame.
    ■ For external use only
    ■ When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
    ■ Stop use and ask a doctor if irritation or rash appears and lasts
    ■ Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • 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.

  • Uses

    Uses:

    Hand sanitizer to help reduce bacteria on the skin that could cause disease

  • Directions

    Directions:

    ■ Place enough product in your palm to thoroughly cover your hands
    ■ Rub hands together briskly until dry
    ■ Children under 6 years of age should be supervised when using this product

  • Other Information

    Other Information
    ■ Do not store above 110℉(43℃)
    ■May discolor certain fabrics or surfaces

  • Questions

    Questions
    www.blifeusa.com

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of bottle

  • INGREDIENTS AND APPEARANCE
    MISSY KAY PREMIUM HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75006-010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL310 g  in 500 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    Methylparaben (UNII: A2I8C7HI9T)  
    Butylene Glycol (UNII: 3XUS85K0RA)  
    Hexylene Glycol (UNII: KEH0A3F75J)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75006-010-01500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E04/01/2020
    Labeler - BLIFE (694894131)
    Registrant - BLIFE (694894131)
    Establishment
    NameAddressID/FEIBusiness Operations
    DongbangCosmetics Co., ltd.694452564manufacture(75006-010)
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