Label: AMMONIA- inhalant aerosol

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated September 2, 2021

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  • ACTIVE INGREDIENT

    Active Ingredients (each inhalant)

    Ammonia (15%)

  • PURPOSE

    Purpose

    Inhalant

  • INDICATIONS & USAGE

    Uses To prevent or treat 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 a 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 1-800-777-4908

  • PRINCIPAL DISPLAY PANEL

    NDC 68599-7100-1

    McKesson
    Ammonia Inhalants
    15% - 35% Strength
    Prevent or Treat Fainting
    Net Contents
    0.01 fl oz
    (0.3 mL)

    MFR# 10104

    BoxDrug factCase

  • INGREDIENTS AND APPEARANCE
    AMMONIA 
    inhalant aerosol
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68599-7100
    Route of AdministrationRESPIRATORY (INHALATION)
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AMMONIA (UNII: 5138Q19F1X) (AMMONIA - UNII:5138Q19F1X) AMMONIA0.15 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    NUTMEG OIL (UNII: Z1CLM48948)  
    WATER (UNII: 059QF0KO0R)  
    LEMON OIL (UNII: I9GRO824LL)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68599-7100-10.15 g in 1 BOX; Type 0: Not a Combination Product01/16/202009/01/2026
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/16/202009/01/2026
    Labeler - McKesson (023904428)
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