Label: AMMONIA INHALANTS inhalant

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

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Drug Label Information

Updated April 14, 2021

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  • Active ingredient(s)

    Ammonia (15%)

  • Purpose

     Inhalant

  • Use(s)

    To prevent or treat fainting

  • Warnings

    Keep away from the Eyes.

    For external use only

    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.

  • Directions

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

  • Other information

     Store at room temperature away from light.

  • Storage

     Store at 20ºC to 25ºC (68ºF to 77ºF)

  • Inactive ingredients

     Alcohol USP, FDC red dye 40, lavender oil fcc, lemon oil fcc, nutmeg oil fcc, purified water usp

  • Questions

     Questions? Call 1-866-390-4411 Mon - Fri 9:00 AM - 5:00 PM

  • Ammonia Inhalants

    Label Image
  • INGREDIENTS AND APPEARANCE
    AMMONIA INHALANTS 
    ammonia inhalants inhalant
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:50090-0342(NDC:39822-9900)
    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
    ALCOHOL (UNII: 3K9958V90M)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    WATER (UNII: 059QF0KO0R)  
    NUTMEG OIL (UNII: Z1CLM48948)  
    LEMON OIL (UNII: I9GRO824LL)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50090-0342-012 in 1 CARTON11/28/2014
    1.3 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 - A-S Medication Solutions (830016429)
    Establishment
    NameAddressID/FEIBusiness Operations
    A-S Medication Solutions830016429RELABEL(50090-0342)
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