Label: JNK YRD ADVANCED HAND SANITIZER LAVENDER SCENT- alcohol liquid

  • NDC Code(s): 74934-088-01, 74934-088-02
  • Packager: Zhejiang iColor Biotech Co., Ltd
  • 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[s]

    Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

  • Warnings

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

    Do not use

    • in children less than 2 months of age
    • on open skin wounds

    When using this product

    keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

    Stop use and ask a doctor

    if irritation or rash occurs. These may be signs of a serious conditions.

    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 hands together until dry.
    ● Supervise children under 6 years of age when using this product to avoid swallowing.

  • Other information

    • Store between 15-30°C (59-86°F)
    • Avoid freezing and excessive heat above 40°C (104°F)
  • Inactive ingredients

    Purified Water USP, Glycerin, Panthenol, Tocopheryl Acetate

  • Package Labeling: 60ml

    Bottle3

  • Package Labeling: 500ml

    Bottle4

  • INGREDIENTS AND APPEARANCE
    JNK YRD ADVANCED HAND SANITIZER LAVENDER SCENT 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74934-088
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74934-088-0160 mL in 1 BOTTLE; Type 0: Not a Combination Product08/10/202101/31/2026
    2NDC:74934-088-02500 mL in 1 BOTTLE; Type 0: Not a Combination Product08/10/202101/31/2026
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)08/10/202101/31/2026
    Labeler - Zhejiang iColor Biotech Co., Ltd (554528308)