OTC Medication Information: Ammonia Inhalants

AMMONIA INHALANTS- ammonia inhalant
James Alexander 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.

Drug Facts

Active Ingredients (each inhalant)

Ammonia (15%)

Purpose

inhalant

Uses

To prevent or treat 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.

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 nostrils of affected person.

Other Information

Store at room temperature away from light.

Inactive Ingredients

Alcohol USP, FD&C Red Dye # 40, Lavender Oil FCC, Lemon Oil FCC, Nutmeg Oil FCC, Purified Water USP.

Questions?

Call 1-908-362-9266 Monday through Friday. 9:00am — 5:00pm e.s.t

DISPENSING SOLUTIONS®


JAMES ALEXANDER CORPORATION
Blairstown, NJ• (908) 362-9266
Product information and MSDS available on-line at:
www.james-alexander.com

Void of Aqueous

Packaging

image description
(click image for full-size original)

Packaging

image description
(click image for full-size original)

AMMONIA INHALANTS
ammonia inhalants inhalant
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:46414-3333
Route of Administration RESPIRATORY (INHALATION) DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
AMMONIA (AMMONIA) AMMONIA 0.045 g in 0.3 mL
Inactive Ingredients
Ingredient Name Strength
ALCOHOL
FD&C RED NO. 40
WATER
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:46414-3333-2 100 AMPULE in 1 CARTON contains a AMPULE (46414-3333-3)
1 NDC:46414-3333-3 0.3 mL in 1 AMPULE This package is contained within the CARTON (46414-3333-2)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 02/14/1976
Labeler — James Alexander Corporation (040756421)
Registrant — James Alexander Corporation (040756421)
Establishment
Name Address ID/FEI Operations
James Alexander Corporation 040756421 manufacture (46414-3333)

Revised: 01/2019 James Alexander Corporation

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Terms of Use | Copyright © 2024. All Rights Reserved.