Label: S PANAX ALL IN ONE MIST- sodium benzoate liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated May 18, 2021

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  • ACTIVE INGREDIENT

    Sodium benzoate

  • INACTIVE INGREDIENT

    Dendropanax morbiferus Extract

  • PURPOSE

    Corona virus, Sterilization, antibacterial, deodorant, fragrance, multi-functional liquid soap

  • WARNINGS

    ■ if following abnormal symptoms persist, discontinue use

    Irritation around the eyes, ears, mucous membranes, including the mouth, under the skin irritation and rashes

    ■ Stop immediately and consult a doctor if you experience

    1) Hypersensitivity symptoms such as erythema, itching and dermatitis.

    2) Skin Irritation

    3) Following Instructions when using medication

    (1) For external use only (Do not use internally)

    (2) Avoid getting into the eyes (if contact occurs, wash well with clean water)

    ■ Be careful not to inhale or use excessively for a long time (ingesting ethanol repeatedly causes irritation to mucous membranes and headaches or other symptoms may appear. When used repeatedly in the same area, skin irritation may occur.

    ■ Do not use the product for a long time in the same area as swelling, inflammation or sickness may occur due to absorption through the skin.

    It is not recommended to use this one areas that have been medically treated with a cast or bandage.

    ■ Do not use in combination with soap or antibacterial cleansing agents.

  • KEEP OUT OF REACH OF CHILDREN

    • Keep Out of Reach of Children.

  • INDICATIONS & USAGE

    ■ Pour a small amount into hands, spread evenly and rub into the skin

  • DOSAGE & ADMINISTRATION

    for topical use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    S PANAX ALL IN ONE MIST 
    sodium benzoate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81885-0002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM BENZOATE (UNII: OJ245FE5EU) (BENZOIC ACID - UNII:8SKN0B0MIM) SODIUM BENZOATE0.5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81885-0002-180 mL in 1 BOTTLE; Type 0: Not a Combination Product05/18/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/18/2021
    Labeler - S AND PANAX CO LTD (695447279)
    Registrant - S AND PANAX CO LTD (695447279)
    Establishment
    NameAddressID/FEIBusiness Operations
    S AND PANAX CO LTD695447279manufacture(81885-0002)