Label: AMMONIA INHALANT- ammonia aerosol

  • 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 20, 2021

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

View All Sections
  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active Ingredients: (Each Inhalant)
    Ammonia 15%

  • PURPOSE

    Purpose
    Inhalant

  • INDICATIONS & USAGE

    Uses: To treat or to prevent fainting.

  • WARNINGS

    Warnings
    For external use only
    Do not use if you have breathing problems such as asthma or emphysema.

  • STOP USE

    Stop use and ask doctor if condition persists

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

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

  • OTHER SAFETY INFORMATION

    Other Information: Store at room temperature away from light.

  • INACTIVE INGREDIENT

    Inactive ingredients: Alcohol USP, FD&C Red Dye #40, Lavender Oil FCC, Lemon Oil FCC, Nutmeg Oil FCC, Purified Water USP.

  • QUESTIONS

    Questions?Call 800-234-1464 Monday – Friday, 8:00am – 8:00pm [ET].

  • PRINCIPAL DISPLAY PANEL

    Reorder No. 10104
    Moore Medical
    Supporting Health & Care
    UPN# 0-0607415-10104-1
    Moore Brand Ammonia Inhalants
    100 Inhalants 0.01 fl. Oz. (0.3mL) each
    Use to prevent fainting
    For inhalation only
    Individually wrapped

    10104 Box

  • INGREDIENTS AND APPEARANCE
    AMMONIA INHALANT 
    ammonia aerosol
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55670-710
    Route of AdministrationRESPIRATORY (INHALATION)
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AMMONIA (UNII: 5138Q19F1X) (AMMONIA - UNII:5138Q19F1X) AMMONIA0.045 g  in 0.3 mL
    Inactive Ingredients
    Ingredient NameStrength
    NUTMEG OIL (UNII: Z1CLM48948)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    ALCOHOL (UNII: 3K9958V90M)  
    LEMON OIL (UNII: I9GRO824LL)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55670-710-01100 in 1 BOX11/29/201701/01/2025
    10.3 mL in 1 CAPSULE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other11/29/201701/01/2025
    Labeler - Moore Medical LLC (051420107)
    Establishment
    NameAddressID/FEIBusiness Operations
    James Alexander Corp.040756421manufacture(55670-710)
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!