Label: AMMONIA PAD- ammonia inhalant

  • 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 April 4, 2011

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  • Content

    One prep pad saturated with 10% ammonia

  • Purpose

    prevent or treat fainting

  • Uses

    Uses to arouse the consciousness of a fainted victim with the vigorous smell of the ammonia in the pad. For external use only.

  • Caution

    Do not swallow. Keep away from eyes; wash with plenty of water if contacted.

  • Inactive Ingredients

    Purified water.

  • Directions

    Tear off a corner and wave it under the victim's nose that has fainted or is on the verge of unconsciousness.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

  • PRINCIPAL DISPLAY PANEL

    Ammonia Inhalant Pad

    GFA Production Xiamen Co., Ltd
    www.gfaproduction.com

    GFA Production Xiamen Co., Ltd
    No. 20 Huli Industrial Park, Meixi Road,
    Tong'an, Xiamen, Fujian, China 361100

    Wellkang Ltd t/a Wellkang Tech Consulting
    Suite B, 29 Harley Street
    LONDON W1G 9QR, England, United Kingdom
  • PRINCIPAL DISPLAY PANEL

    Ammonia Inhalant Pads

  • PRINCIPAL DISPLAY PANEL

    Ammonia Inhalant Pads

  • INGREDIENTS AND APPEARANCE
    AMMONIA PAD 
    ammonia inhalant
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52124-3201
    Route of AdministrationRESPIRATORY (INHALATION)
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AMMONIA (UNII: 5138Q19F1X) (AMMONIA - UNII:5138Q19F1X) AMMONIA10 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52124-3201-10.5 mL in 1 PACKET
    2NDC:52124-3201-2100 in 1 BOX
    20.5 mL in 1 PACKET
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other04/04/2011
    Labeler - Genuine First Aid, LLC (619609857)