Label: LIFE Q- sodium bicarbonate tablet

  • 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 November 2, 2021

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  • Active ingredient[s]

    Sodium bicarbonate 60%

  • Purpose

    Hand Sanitizer

  • Use[s]

    Virus, bacteria, bacteria removal and infection prevention effect from all spaces and objects in daily life.

    Recommended for repeated use.

  • Warinings

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

  • Do not use

    • Do not eat.
    • Do not spray directly on the body.
  • When using this product

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

  • In case of adverse skin reactions

    visit a hospital and follow your doctor's instructions.

  • Keep out of reach of children.

  • Directions

    • Put 1 tablet of disinfectant in 2 liters of water and wait for 2 minutes.
    • Put it in a sprayer and spray an appropriate amount on the area where virus, bacteria, and bacteria need to be sterilized.
    • It is recommended to use 1 tablet of disinfectant in an electric sprayer with a capacity of 2L to 3L.
  • Other information

    • Sealed storage lengthens the storage period.
    • Avoid direct sunlight and store in a cool dry place.
  • Inactive ingredients

    Sodium chlorite, Sodium sulfite, Citric acid, Maleic acid

  • Package Label

    20g NDC: 80760-201-01 Label

  • INGREDIENTS AND APPEARANCE
    LIFE Q 
    sodium bicarbonate tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80760-201
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) (BICARBONATE ION - UNII:HN1ZRA3Q20) SODIUM BICARBONATE60 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORITE (UNII: G538EBV4VF)  
    SODIUM SULFITE (UNII: VTK01UQK3G)  
    MALEIC ACID (UNII: 91XW058U2C)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize12mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80760-201-0120 g in 1 BOTTLE; Type 0: Not a Combination Product10/12/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other10/12/2020
    Labeler - Saenggi Life (695012496)
    Registrant - Saenggi Life (695012496)
    Establishment
    NameAddressID/FEIBusiness Operations
    Saenggi Life695012496manufacture(80760-201)