Label: AMMONIASPORT RAW- ammonia 2% 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 September 18, 2020

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

  • WARNINGS AND PRECAUTIONS

     Drug Facts

  • Active Ingredient

    Ammonia 2 %

  • Purpose

     Respiratory Stimulant

  • Use

    Respiratory stimulant used as a smelling salts to treat or prevent fainting.

  • Warnings

     For external use only. Avoid eye contact with liquid vapors. Avoid inhaling more than a slight whiff. May cause irritation if excess is inhaled.

  • If pregnant or nursing a baby

     seek the advice of a doctor before using this product.

  • Keep out of the reach of children

     In case of accidental ingestion, seek professional assistance or contact a Poison Control Center right away.

  • Directions

    Inhale a slight whiff to treat a "fainting spell"

  • Inactive Ingredients

    Ammonium Carbonate, Sodium Carbonate

  • Other Information

    Flammable: Keep away from spark, heat or flame. Keep tightly closed at room temperature not to exceed 30C (86F).

  • Questions or Comments?

     1-800-662-3435

  • Label

    Label RAW

    31 ml NDC 73395-197

  • INGREDIENTS AND APPEARANCE
    AMMONIASPORT RAW 
    ammonia 2% liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73395-197
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AMMONIA (UNII: 5138Q19F1X) (AMMONIA - UNII:5138Q19F1X) AMMONIA20 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    AMMONIUM CARBONATE (UNII: NJ5VT0FKLJ)  
    SODIUM CARBONATE (UNII: 45P3261C7T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73395-197-0131 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/01/2020
    Labeler - AmmoniaSport LLC (048476710)
    Registrant - AmmoniaSport LLC (048476710)
    Establishment
    NameAddressID/FEIBusiness Operations
    James Alexander Corp040756421manufacture(73395-197)