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
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Updated March 13, 2013
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- Active ingredient (each inhalant)
To arouse consciousness and restore mental alertness.Close
For external use only
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Hold inhalant away from face and crush between thumb and forefinger. Carefully approach crushed inhalant to nostril until desired effect is achieved.Close
- Other information
Store at room temperature away from light.Close
- Inactive ingredients
Alcohol USP, Eucalyptus Oil, FD and C Blue Dye #1, Lemon Oil, Purified Water USP, Rosemary OilClose
- PRINCIPAL DISPLAY PANEL
- INGREDIENTS AND APPEARANCE
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53063-1112 Route of Administration RESPIRATORY (INHALATION) Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIA (UNII: 5138Q19F1X) (AMMONIA - UNII:5138Q19F1X) AMMONIA 0.013 mL in 0.3 mL Inactive Ingredients Ingredient Name Strength 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 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)