Label: GO TIME - ammonia inhalant

  • NDC Code(s): 53063-1112-1, 53063-1112-2
  • Packager: Mountain Top Labs, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated 03/13

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

  • Active ingredient (each inhalant)

    Ammonia 4.5%

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  • Purpose

    Reflex Stimulant

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  • Uses

    To arouse consciousness and restore mental alertness.

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  • 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.

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  • Directions

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

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  • Other information

    Store at room temperature away from light.

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  • Inactive ingredients

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

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  • Questions?

    Call 1-801-448-6809

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  • PRINCIPAL DISPLAY PANEL

    NDC 53063-1112-1

    NDC 53063-1112-1

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  • INGREDIENTS AND APPEARANCE
    GO TIME 
    ammonia inhalant
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:53063-1112
    Route of Administration RESPIRATORY (INHALATION) DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    AMMONIA (AMMONIA) AMMONIA 0.013 mL  in 0.3 mL
    Inactive Ingredients
    Ingredient Name Strength
    ALCOHOL  
    EUCALYPTUS OIL  
    FD&C BLUE NO. 1  
    LEMON OIL  
    WATER  
    ROSEMARY OIL  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:53063-1112-2 4 in 1 BOX
    1 NDC:53063-1112-1 0.3 mL in 1 AMPULE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 08/13/2012
    Labeler - Mountain Top Labs, LLC (078408468)
    Establishment
    Name Address ID/FEI Business Operations
    Omniglow de Mexico, S.A. de C .V. 589918408 manufacture(53063-1112)
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