Label: GO TIME- ammonia inhalant
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Contains inactivated NDC Code(s)
NDC Code(s): 53063-1112-1, 53063-1112-2 - Packager: Mountain Top Labs, LLC
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated March 13, 2013
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- Active ingredient (each inhalant)
- Purpose
- Uses
- Warnings
- Directions
- Other information
- Inactive ingredients
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- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
GO TIME
ammonia inhalantProduct 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)