AMMONIA INHALANTS inhalant

Ammonia Inhalants by

Drug Labeling and Warnings

Ammonia Inhalants by is a Otc medication manufactured, distributed, or labeled by James Alexander Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

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

SPL UNCLASSIFIED SECTION

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

Packaging

INGREDIENTS AND APPEARANCE

AMMONIA INHALANTS 
ammonia inhalants inhalant

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 46414-3333
Route of Administration	RESPIRATORY (INHALATION)

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMMONIA (UNII: 5138Q19F1X) (AMMONIA - UNII:5138Q19F1X)	AMMONIA	0.045 g  in 0.3 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
FD&C RED NO. 40 (UNII: WZB9127XOA)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 46414-3333-2	100 in 1 CARTON	02/14/1976
1	NDC: 46414-3333-3	0.3 mL in 1 AMPULE; Type 0: Not a Combination Product

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	Business Operations
James Alexander Corporation		040756421	manufacture(46414-3333)