Active Ingredient (Each Inhalant)
Ammonia 4.5%
Go Time
FDA Label NDC 53063-1113
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Mountain Top Labs, Llc for the product Go Time (NDC 53063-1113). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient (each inhalant), purpose, uses, warnings, otc - do not use, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Reflex Stimulant
Uses
To arouse consciousness and restore mental alertness.
Warnings
For external use only
Otc - Do Not Use
Do not use if you have breathing problems such as asthma or emphysema.
Otc - When Using
When using this product avoid contact with the eyes.
Otc - Stop Use
Stop use and ask a doctor if you experience any adverse effects.
Otc - Keep Out Of Reach Of Children
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
Package Label.Principal Display Panel
NDC 53063-1113-1
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