AMMONIA INHALANTS inhalant

Ammonia Inhalants by

Drug Labeling and Warnings

Ammonia Inhalants by is a Prescription medication manufactured, distributed, or labeled by X-GEN Pharmaceuticals, Inc., X-Gen Pharmaceuticals, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient(s)

Ammonia (15%)

Purpose

 Inhalant

Use(s)

To prevent or treat fainting

Warnings

Keep away from the Eyes.

For external use only

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

 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.

Storage

 Store at 20ºC to 25ºC (68ºF to 77ºF)

Inactive ingredients

 Alcohol USP, FDC red dye 40, lavender oil fcc, lemon oil fcc, nutmeg oil fcc, purified water usp

Questions

 Questions? Call 1-866-390-4411 Mon - Fri 9:00 AM - 5:00 PM

Principal Display Panel

Ampule Label

10 ampule carton

 

12 ampule carton

INGREDIENTS AND APPEARANCE

AMMONIA INHALANTS 
ammonia inhalants inhalant

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 39822-9900
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)
LAVENDER OIL (UNII: ZBP1YXW0H8)
WATER (UNII: 059QF0KO0R)
NUTMEG OIL (UNII: Z1CLM48948)
LEMON OIL (UNII: I9GRO824LL)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 39822-9900-1	10 in 1 CARTON
1		0.3 mL in 1 AMPULE
2	NDC: 39822-9900-2	12 in 1 CARTON
2		0.3 mL in 1 AMPULE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
UNAPPROVED DRUG OTHER		02/14/1976

Labeler - X-GEN Pharmaceuticals, Inc. (790169531)

Registrant - X-Gen Pharmaceuticals, Inc. (790169531)