Label: WHENEVER HAND PURIFYING- ethanol gel

  • Category: HUMAN OTC DRUG LABEL

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 December 7, 2020

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  • ACTIVE INGREDIENT

    Ethanol 62 % v/v

  • INACTIVE INGREDIENTS

    D.I Water, Glycerin, 1.3BG, Cabopol EEG 940, Sodium Hyaluronate(0.5%), Aloe Extract, Tromethamine(20%)

  • PURPOSE

    Antiseptic

  • WARNINGS

    For external use only-hands
    Flammable. Please keep away from heat and flame.

    When using this product ■ Keep out of eyes. In case of contact with eyes, flush thoroughly with water. ■ Avoid contact with damaged skin. ■ Do not inhale or ingest.

    Stop use and ask a doctor if skin irritation or rash develops.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

  • KEEP OUT OF REACH OF CHILDREN

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

  • Uses

    ■ Hand sanitizer to decrease bacteria on hands which may cause disease

  • Directions

    ■ Squeeze out the contents from the pack and rub softly on hands to cover all surfaces and nails. Continue rub hands smoothly until they dried.
    ■ Supervise thoroughly children when they use not to swallowing.

  • Other information

    ■ Store between 50F~86F (10C~30C)
    ■ Avoid freezing and excessive heat above 40C (104F)

  • QUESTIONS

    If you have any question about this product, please phone to +82-32-715-7881 or email to; sanitizerinpocket@gmail.com

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of carton

  • INGREDIENTS AND APPEARANCE
    WHENEVER HAND PURIFYING 
    ethanol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:90038-010
    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)  
    Glycerin (UNII: PDC6A3C0OX)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    ALOE (UNII: V5VD430YW9)  
    TROMETHAMINE (UNII: 023C2WHX2V)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:90038-010-0240 in 1 CARTON12/01/2020
    1NDC:90038-010-013 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A12/01/2020
    Labeler - JoyunCostech (694039775)
    Registrant - JoyunCostech (694039775)
    Establishment
    NameAddressID/FEIBusiness Operations
    JoyunCostech694039775manufacture(90038-010)
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