Otc - Active Ingredient
active ingredient each inhalant purpose ammonia 15% inhalant
Ammonia Inhalants Inhalant
FDA Label NDC 67777-251
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dynarex Corporation for the product Ammonia Inhalants (NDC 67777-251). 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 otc - active ingredient, otc - purpose, otc - keep out of reach of children, dosage & administration, storage and handling, inactive ingredient, indications & usage, warnings, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Uses to prevent or treating fainting
warnings for external use only
do not use if you have breathing problems such as asthma or emphysema
stop use and ask a doctor if condition persists
Otc - Keep Out Of Reach Of Children
If swallowed get medical help or contact a Poison Control Center right away
Dosage & Administration
Hold inhalant away from face and crush between thumb and forefinger. carefully approach crushed inhalant to nostrils of affected person.
Storage And Handling
Store at room temperature away from light
Inactive Ingredient
alcohol fdc red dye 40 lavender oil, lemon oil, nutmeg oil, purified water usp
Indications & Usage
to prevent or treat fainting
Warnings
for external use only
Package Label.Principal Display Panel
ammonia inhalants
a respiratory stimulant for inhalation only latex free
Box Label (Box1401 01)
* Please review the disclaimer below.
