AMMONIA INHALANTS- ammonia inhalant

Ammonia Inhalants by

Drug Labeling and Warnings

Ammonia Inhalants by is a Otc medication manufactured, distributed, or labeled by HART Health. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient: Ammonia 15%

PURPOSE

Purpose:

Reflex Stimulant

INDICATIONS & USAGE

Uses:

to aid in prevention and treatment of fainting

WARNINGS

Warnings:

For external use only

Flammable, keep away from heat or flame

DO NOT USE

Do not use:

• if face is flush
• in or near the eyes
• if you have breathing problems such as asthma or emphysema

STOP USE

Stop use and ask a doctor if:

• patient is non-responsive
• condition lasts

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. 1-800-1222

DOSAGE & ADMINISTRATION

Adults and children 12 years of age and older:

• hold away from face and crush inhalant between fingers
• hold packet six inches from patient's nose
• gradually move inhalant closer until patient revives
• check strength frequently by holding near your own nose
• if necessary, use another when first is expended
• dispose of properly

Children under 12 years of age: ask a doctor

INACTIVE INGREDIENT

Inactive ingredients: alcohol USP, FD&C red dye #40, lavender oil FCC, lemon oil FCC, nutmeg oil FCC, purified water USP

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

AMMONIA INHALANTS 
ammonia inhalant

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50332-0054
Route of Administration	RESPIRATORY (INHALATION)

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMMONIA (UNII: 5138Q19F1X) (AMMONIA - UNII:5138Q19F1X)	AMMONIA	0.15 g  in 1 g

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: 50332-0054-1	10 in 1 BOX	01/04/2021
1		.15 g 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		01/01/2000

Labeler - HART Health (069560969)