Label: GO TIME- ammonia inhalant

  • NDC Code(s): 53063-1113-1, 53063-1113-2
  • Packager: Mountain Top Labs, 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 September 28, 2012

If you are a consumer or patient please visit this version.

  • Active ingredient (each inhalant)

    Ammonia 4.5%

  • Purpose

    Reflex Stimulant

  • Uses

    To arouse consciousness and restore mental alertness.

  • Warnings

    For external use only

    Do not use if you have breathing problems such as asthma or emphysema.

    When using this product avoid contact with the eyes.

    Stop use and ask a doctor if you experience any adverse effects.

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

  • Directions

    Hold inhalant away from face and crush between thumb and forefinger.  Carefully approach crushed inhalant to nostril until desired effect is achieved.

  • Other information

    Store at room temperature away from light.

  • Inactive ingredients

    Alcohol USP, Cinnamon Cassia Oil, Eucalyptus Oil, FD and C Blue Dye #1, Purified Water USP

  • Questions?

    Call 1-801-448-6809

  • PRINCIPAL DISPLAY PANEL

    NDC 53063-1113-1

    NDC 53063-1113-1

  • INGREDIENTS AND APPEARANCE
    GO TIME 
    ammonia inhalant
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53063-1113
    Route of AdministrationRESPIRATORY (INHALATION)
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AMMONIA (UNII: 5138Q19F1X) (AMMONIA - UNII:5138Q19F1X) AMMONIA0.013 mL  in 0.3 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    CINNAMON OIL (UNII: E5GY4I6YCZ)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53063-1113-24 in 1 BOX
    1NDC:53063-1113-10.3 mL in 1 AMPULE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other08/13/2012
    Labeler - Mountain Top Labs, LLC (078408468)