Label: NARO AMOR- potassium carbonate liquid

  • Category: OTC ANIMAL 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 October 5, 2021

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  • ACTIVE INGREDIENT

    Potassium carbonate

  • INACTIVE INGREDIENT

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

  • PURPOSE

    Sanitizer to help decrease bacteria on skin

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

  • INDICATIONS & USAGE

    Spray on the skin (animal) as needed

  • WARNINGS

    Use only according to instructuins.

    Keep out of reach of children.

    Avoid contact with eyes.

    In case of eye contact, flush thoroughly with water.

  • DOSAGE & ADMINISTRATION

    For external use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    NARO AMOR 
    potassium carbonate liquid
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:81936-0004
    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
    WATER (UNII: 059QF0KO0R)  
    CALCIUM HYDROXIDE (UNII: PF5DZW74VN)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81936-0004-1500 mL in 1 BOTTLE, SPRAY
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/30/2021
    Labeler - NARO Global Inc. (695123340)
    Establishment
    NameAddressID/FEIBusiness Operations
    NARO Global Inc.695123340manufacture, api manufacture, label