Label: SANITALK GREEN - FRUIT ,VEGETABLE- potassium carbonate 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 January 14, 2022

If you are a consumer or patient please visit this version.

View All Sections
  • ACTIVE INGREDIENT

    potassium carbonate

  • INACTIVE INGREDIENT

    ε-Polylysine.Dextrin.1,2-Propanediol.Citric Acid.Tea Catechin. Hydroxypropylmethyl Cellulose.Distilled water.

  • PURPOSE

    Helps to kill bacteria and germs on foods, and remove harmful residues on meats and vegetables.

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    For hygienic disinfection, this product can be used directly to the surface. Also, you can dilute one part product with two parts water

  • WARNINGS

    For external use only.

    When using this product

    Avoid contact with eyes. Discontinue use if signs of irritation or rashes appear.

    Keep out of reach of children.

    Store at room temperature.

  • DOSAGE & ADMINISTRATION

    for external use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    SANITALK GREEN - FRUIT ,VEGETABLE 
    potassium carbonate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82486-0002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POTASSIUM CARBONATE (UNII: BQN1B9B9HA) (CARBONATE ION - UNII:7UJQ5OPE7D) POTASSIUM CARBONATE0.1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82486-0002-1500 mL in 1 BOTTLE; Type 0: Not a Combination Product01/12/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/12/2022
    Labeler - Sanitalk Inc (695365740)
    Registrant - Sanitalk Inc (695365740)
    Establishment
    NameAddressID/FEIBusiness Operations
    NARO Global Inc.695123340manufacture(82486-0002)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!