Label: AMMONIA INHALANTS inhalant

  • Category: HUMAN OTC DRUG LABEL

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 April 27, 2023

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • ACTIVE INGREDIENT

    active ingredient each inhalant purpose ammonia 15% inhalant

  • PURPOSE

    Uses to prevent or treating fainting

    warnings for external use only

    do not use if you have breathing problems such as asthma or emphysema

    stop use and ask a doctor if condition persists

  • KEEP OUT OF REACH OF CHILDREN

    If swallowed get medical help or contact a Poison Control Center right away

  • DOSAGE & ADMINISTRATION

    Hold inhalant away from face and crush between thumb and forefinger.  carefully approach crushed inhalant to nostrils of affected person.

  • STORAGE AND HANDLING

    Store at room temperature away from light

  • INACTIVE INGREDIENT

    alcohol fdc red dye 40 lavender oil, lemon oil, nutmeg oil, purified water usp

  • INDICATIONS & USAGE

    to prevent or treat fainting

  • WARNINGS

    for external use only

  • PRINCIPAL DISPLAY PANEL

    NDC 71872-7261-01

    5 X 0.33cc Ampules

    Ammonia inhalants

    A respiratory stimulant for inhalation only latex free

    Latex Free

    Alcohol 35%

    Ammonia 15%

    71872-7261-5.PDP

  • INGREDIENTS AND APPEARANCE
    AMMONIA INHALANTS 
    ammonia inhalants inhalant
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71872-7261(NDC:67777-251)
    Route of AdministrationRESPIRATORY (INHALATION)
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AMMONIA (UNII: 5138Q19F1X) (AMMONIA - UNII:5138Q19F1X) AMMONIA0.05 g  in 0.33 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71872-7261-55 in 1 BAG07/07/2021
    10.33 mL in 1 AMPULE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other02/14/197610/31/2025
    Labeler - Medical Purchasing Solutions, LLC (601458529)
    Establishment
    NameAddressID/FEIBusiness Operations
    Medical Purchasing Solutions, LLC601458529repack(71872-7261)