Label: FIRST AID ONLY AMMONIA INHALANTS- ammonia inhalants inhalant

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

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Drug Label Information

Updated February 19, 2018

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  • ACTIVE INGREDIENT

    Active Ingredient

    Ammonia(15%)

  • PURPOSE

    Purpose

    Aromatic Stimulant

  • 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 and ask a doctor if condition persists

  • KEEP OUT OF REACH OF CHILDREN

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

  • DOSAGE & ADMINISTRATION

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

  • INFORMATION FOR PATIENTS

    Other Information Store at room temperarure, away from light

  • INACTIVE INGREDIENT

    Inactive Ingredients Alcohol USP, FD&C Red Dye #40, Lavender Oil NF, Lemon Oil NF, Nutmeg Oil NF, Purified Water USP

  • QUESTIONS

    Questions 1.800.835.2263

  • PRINCIPAL DISPLAY PANEL

    Carton Image

  • INGREDIENTS AND APPEARANCE
    FIRST AID ONLY AMMONIA INHALANTS 
    ammonia inhalants inhalant
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0924-5401(NDC:46414-3333)
    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
    LEMON OIL (UNII: I9GRO824LL)  
    WATER (UNII: 059QF0KO0R)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    ALCOHOL (UNII: 3K9958V90M)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    NUTMEG OIL (UNII: Z1CLM48948)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0924-5401-0110 in 1 CARTON01/01/2006
    10.3 mL in 1 AMPULE; Type 0: Not a Combination Product
    2NDC:0924-5401-02100 in 1 CARTON01/01/2006
    20.3 mL in 1 AMPULE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/01/2006
    Labeler - Acme United Corporation (001180207)
    Registrant - Acme United Corporation (001180207)
    Establishment
    NameAddressID/FEIBusiness Operations
    Acme United Corporation045924339relabel(0924-5401) , repack(0924-5401)
    Establishment
    NameAddressID/FEIBusiness Operations
    Acme United Corporation080119599relabel(0924-5401) , repack(0924-5401)
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