AMMONIA INHALANTS- ammonia inhalants inhalant 
Dynarex Corporation

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.


1401 Ammonia Inhalants (Ampule) NDC 67777-251-01

active ingredient each inhalant purpose ammonia 15% inhalant

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

If swallowed get medical help or contact a Poison Control Center right away

Hold inhalant away from face and crush between thumb and forefinger.  carefully approach crushed inhalant to nostrils of affected person.

Store at room temperature away from light

alcohol fdc red dye 40 lavender oil, lemon oil, nutmeg oil, purified water usp

to prevent or treat fainting

for external use only

ammonia inhalants

a respiratory stimulant for inhalation only latex free

box label

ammonia inhalants inhalant
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-251
Route of AdministrationRESPIRATORY (INHALATION)
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AMMONIA (UNII: 5138Q19F1X) (AMMONIA - UNII:5138Q19F1X) AMMONIA0.05 g  in 0.33 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67777-251-010.33 mL in 1 AMPULE; Type 0: Not a Combination Product02/14/1976
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other02/14/1976
Labeler - Dynarex Corporation (008124539)
Registrant - Dynarex Corporation (008124529)

Revised: 5/2023
Document Id: fb4831ed-91ce-c9ed-e053-6394a90a045a
Set id: 91e27f1c-0f74-413e-97ff-2fc013f22ca8
Version: 3
Effective Time: 20230509
Dynarex Corporation