Label: AMMONIA INHALANTS inhalant

  • 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 May 9, 2023

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

View All Sections
  • 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


    ammonia inhalants


    a respiratory stimulant for inhalation only latex free

    box label

  • 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:67777-251-010.33 mL in 1 AMPULE; Type 0: Not a Combination Product02/14/1976
    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)
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!