Label: GO TIME- ammonia inhalant

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

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Drug Label Information

Updated March 13, 2013

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  • 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, Eucalyptus Oil, FD and C Blue Dye #1, Lemon Oil, Purified Water USP, Rosemary Oil

  • Questions?

    Call 1-801-448-6809

  • PRINCIPAL DISPLAY PANEL

    NDC 53063-1112-1

    NDC 53063-1112-1

  • INGREDIENTS AND APPEARANCE
    GO TIME 
    ammonia inhalant
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53063-1112
    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)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    LEMON OIL (UNII: I9GRO824LL)  
    WATER (UNII: 059QF0KO0R)  
    ROSEMARY OIL (UNII: 8LGU7VM393)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53063-1112-24 in 1 BOX
    1NDC:53063-1112-10.3 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)
    Establishment
    NameAddressID/FEIBusiness Operations
    Omniglow de Mexico, S.A. de C .V.589918408manufacture(53063-1112)
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