Label: PREVAIL HAND SANITIZER WITH MOISTURIZERS AND VITAMIN E- alcohol gel

  • NDC Code(s): 79446-028-01, 79446-028-02, 79446-028-03, 79446-028-04
  • Packager: Major Surplus And Survival Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 24, 2024

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

  • Drug Facts

  • Active Ingredient

    Ethyl Alcohol 75% v/v

    Purpose

    Antiseptic

  • Uses

    ● For hand washing to help reduce bacteria that potentially can cause disease. Recommended for repeated use. For use when soap and water are  not available.

  • Warnings

    For external use only. Flammable. Keep away from heat or flame

    Do not use

    • On children less than 2 months of age
    • On open skin wounds

    When using this product

    do not use in or near eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly wit hwater

    Stop use and ask a doctor

    if irritation or rash appears on the skin

    Keep out of reach of children.

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

  • Directions

    ● Place enough product on hands to cover all surfaces. Rub handst ogether until dry. 

    ● Children under 6 years of age should be supervised by adult when applying this product. 

  • Other information

    • Store between 15-30C (59-86F)
    • Avoid freezing and excessive heat above 40C (104F) 
    • May discolor certain fabrics or surfaces
  • Inactive ingredients

    Water, Glycerin, Squalane, Panthenol, Inulin, Sodium Hyaluronate, Fructose, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol.

  • Package Labeling: 60ml

    Box

  • Package Labeling: 250ml

    Box2

  • Package Labeling: 500ml

    Box3

  • Package Labeling: 1000ml

    Box4

  • INGREDIENTS AND APPEARANCE
    PREVAIL HAND SANITIZER WITH MOISTURIZERS AND VITAMIN E 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79446-028
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.75 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SQUALANE (UNII: GW89575KF9)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    INULIN (UNII: JOS53KRJ01)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    FRUCTOSE (UNII: 6YSS42VSEV)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79446-028-0160 mL in 1 BOTTLE; Type 0: Not a Combination Product07/16/202001/31/2026
    2NDC:79446-028-02250 mL in 1 BOTTLE; Type 0: Not a Combination Product07/16/202001/31/2026
    3NDC:79446-028-03500 mL in 1 BOTTLE; Type 0: Not a Combination Product07/16/202001/31/2026
    4NDC:79446-028-041000 mL in 1 BOTTLE; Type 0: Not a Combination Product07/16/202001/31/2026
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)07/16/202001/31/2026
    Labeler - Major Surplus And Survival Inc. (789081502)