Label: AMMONIA INHALANTS inhalant

  • NDC Code(s): 0273-0104-10
  • Packager: YOUNG DENTAL MANUFACTURING CO 1, LLC
  • 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 January 3, 2023

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  • Actives

    Ammonia 15 percent

  • Purpose

    Inhalant

  • Usage

    To treat or prevent fainting. 

  • Warnings

    For External Use Only. 

    Stop use and ask a doctor if condition persists. Do not use if you have breathing problems such as asthma or emphysema.

  • Keep out of reach of children

    If swallowed get medical help or contact a Poison Control Center immediately.

  • Dosage and Administration

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

  • Inactives

    Alcohol USP, FDC red dye 40, Lavender oil fcc, Lemon oil fcc, Nutmeg oil fcc, Purified water usp

  • Product Label

    product label

  • INGREDIENTS AND APPEARANCE
    AMMONIA INHALANTS 
    ammonia inhalants inhalant
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0273-0104
    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)  
    LEMON OIL (UNII: I9GRO824LL)  
    LAVANDIN OIL (UNII: 9RES347CKG)  
    NUTMEG OIL (UNII: Z1CLM48948)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0273-0104-100.3 mL in 1 AMPULE; Type 0: Not a Combination Product01/10/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/09/2018
    Labeler - YOUNG DENTAL MANUFACTURING CO 1, LLC (006309355)
    Registrant - YOUNG DENTAL MANUFACTURING CO 1, LLC (006309355)