Otc - Active Ingredient
Active Ingredients (each inhalant)
Ammonia (15%)
Ammonia Aerosol
FDA Label NDC 68599-7100
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Mckesson for the product Ammonia (NDC 68599-7100). 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, indications & usage, warnings, otc - stop use, otc - keep out of reach of children, dosage & administration, other safety information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose
Inhalant
Indications & Usage
Uses To prevent or treat fainting.
Warnings
Warnings
For external use only.
Do not use if you have breathing problems such as asthma or emphysema.
Otc - Stop Use
Stop use and ask a doctor if condition persists.
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.
Dosage & Administration
Directions Hold inhalant away from face and crush between thumb and forefinger. Carefully
approach crushed inhalant to nostrils of affected person.
Other Safety Information
Other Information Store at room temperature away from light.
Inactive Ingredient
Inactive Ingredients Alcohol USP, FD&C Red Dye # 40, Lavender Oil FCC, Lemon Oil FCC,
Nutmeg Oil FCC, Purified Water USP.
Otc - Questions
Questions? Call 1-800-777-4908
Package Label.Principal Display Panel
NDC 68599-7100-1
McKesson
Ammonia Inhalants
15% - 35% Strength
Prevent or Treat Fainting
Net Contents
0.01 fl oz
(0.3 mL)
MFR# 10104
* Please review the disclaimer below.
