Label: WISH HAND SANITIZER WATERMELON SUGAR- alcohol gel

  • NDC Code(s): 71611-095-01, 71611-095-02, 71611-095-03, 71611-095-04
  • Packager: CLICK PRODUCTS LLC
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated June 27, 2024

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  • ACTIVE INGREDIENT

    Active Ingredient:

    Ethyl Alcohol 70% v/v

  • PURPOSE

    Purpose

    Antimicrobial

  • INDICATIONS & USAGE

    USE: · Hand sanitizer to help reduce bacteria on the skin that may cause disease.

  • WARNINGS

    Warnings: for external use only.

    Flammable. Keep away from heat and flame.

  • WHEN USING

    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

    Stop use and ask a doctor if

    · irritation or redness develops.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. if swallowed, get medical help or contact a poison control center.

  • DOSAGE & ADMINISTRATION

    Directions

    · spray enough product in your palm to thoroughly cover your hands.

    · rub hands together briskly until dry. Recommended for repeated use.

    · children under 6years of age should be supervised when using this product.

  • INACTIVE INGREDIENT

    Inactive Ingredients: · Water(Aqua), Glycerin, Carbomer, Aminomethyl Propanol, Fragrance, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate.

  • PRINCIPAL DISPLAY PANEL

    ITEM#60350
    Watermelon Sugar
    1.2 FL OZ. (35ml)
    NDC: 71611-095-01

    WS 60350 35ml label

  • PRINCIPAL DISPLAY PANEL

    ITEM#60351
    Watermelon Sugar
    1.2 FL OZ. (35ml)
    NDC: 71611-095-02

    WS 60351 35ml label

  • PRINCIPAL DISPLAY PANEL

    ITEM#60352
    Watermelon Sugar
    1.5 FL OZ. (45ml)
    NDC: 71611-095-03

    WS 60352 45ml label

  • PRINCIPAL DISPLAY PANEL

    ITEM#60353
    Watermelon Sugar
    1.5 FL OZ. (45ml)
    NDC: 71611-095-04

    WS 60353 45ml label

  • INGREDIENTS AND APPEARANCE
    WISH HAND SANITIZER WATERMELON SUGAR 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71611-095
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71611-095-011 in 1 BAG06/28/2024
    135 mL in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:71611-095-0235 mL in 1 BOTTLE; Type 0: Not a Combination Product06/28/2024
    3NDC:71611-095-031 in 1 BAG06/28/2024
    345 mL in 1 BOTTLE; Type 0: Not a Combination Product
    4NDC:71611-095-0445 mL in 1 BOTTLE; Type 0: Not a Combination Product06/28/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)06/28/2024
    Labeler - CLICK PRODUCTS LLC (080766174)
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