Active Ingredient(S)
Ammonia (15%)
Ammonia Inhalants
FDA Label NDC 70385-2003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sina Health Inc for the product Ammonia Inhalants (NDC 70385-2003). 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(s), purpose, use(s), warnings, stop use and ask a doctor if, keep out of reach of children, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Inhalant
Use(S)
To prevent or treat fainting
Warnings
Keep away from the Eyes.
Stop Use And Ask A Doctor If
condition persists
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Directions: hold inhalant away from face and crush between thumb and forefinger. Carefully approach crushed inhalant to nostrils of affected person.
Other Information
Store at room temperature away from light.
Storage
Store at 20°C to 25°C (68°F to 77°F)
Inactive Ingredients
Alcohol USP, FDC red dye 40, lavender oil fcc, lemon oil fcc, nutmeg oil fcc, purified water usp
Questions
Questions? Call 1-866-390-4411 Mon - Fri 9:00 AM - 5:00 PM
Principal Display Panel
Pdp (2003 3)
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