AMMONIA INHALANT- ammonia aerosol

Ammonia Inhalant by

Drug Labeling and Warnings

Ammonia Inhalant by is a Otc medication manufactured, distributed, or labeled by Moore Medical LLC, James Alexander Corp.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active Ingredients: (Each Inhalant)
Ammonia 15%

PURPOSE

Purpose
Inhalant

INDICATIONS & USAGE

Uses: To treat or to prevent fainting.

WARNINGS

Warnings
For external use only
Do not use if you have breathing problems such as asthma or emphysema.

STOP USE

Stop use and ask 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.

DOSAGE & ADMINISTRATION

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

OTHER SAFETY INFORMATION

Other Information: Store at room temperature away from light.

INACTIVE INGREDIENT

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

QUESTIONS

Questions?Call 800-234-1464 Monday – Friday, 8:00am – 8:00pm [ET].

PRINCIPAL DISPLAY PANEL

Reorder No. 10104
Moore Medical
Supporting Health & Care
UPN# 0-0607415-10104-1
Moore Brand Ammonia Inhalants
100 Inhalants 0.01 fl. Oz. (0.3mL) each
Use to prevent fainting
For inhalation only
Individually wrapped

INGREDIENTS AND APPEARANCE

AMMONIA INHALANT 
ammonia aerosol

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55670-710
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
NUTMEG OIL (UNII: Z1CLM48948)
FD&C RED NO. 40 (UNII: WZB9127XOA)
LAVENDER OIL (UNII: ZBP1YXW0H8)
ALCOHOL (UNII: 3K9958V90M)
LEMON OIL (UNII: I9GRO824LL)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55670-710-01	100 in 1 BOX	11/29/2017
1		0.3 mL in 1 CAPSULE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		11/29/2017

Labeler - Moore Medical LLC (051420107)

Establishment
Name	Address	ID/FEI	Business Operations
James Alexander Corp.		040756421	manufacture(55670-710)