Label: AMMONIA INHALANTS inhalant

  • NDC Code(s): 67777-251-01, 67777-251-02
  • Packager: Dynarex Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated October 28, 2024

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  • 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

  • Label

    1401 BX MASTER1401 Ammonia Inhalants

  • INGREDIENTS AND APPEARANCE
    AMMONIA INHALANTS 
    ammonia inhalants inhalant
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)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:67777-251-02500 in 1 CASE02/14/1976
    1NDC:67777-251-0110 in 1 BOX
    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 other02/14/1976
    Labeler - Dynarex Corporation (008124539)
    Registrant - Dynarex Corporation (008124529)