FIRST AID ONLY AMMONIA INHALANTS- ammonia inhalants inhalant

First Aid Only Ammonia Inhalants by

Drug Labeling and Warnings

First Aid Only Ammonia Inhalants by is a Otc medication manufactured, distributed, or labeled by Acme United Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Ammonia(15%)

PURPOSE

Purpose

Aromatic Stimulant

INDICATIONS & USAGE

Uses To prevent or treat fainting

WARNINGS

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 the reach of children. If swallowed, get medical help or contact a Poison Control Center immediately

DOSAGE & ADMINISTRATION

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

INFORMATION FOR PATIENTS

Other Information Store at room temperarure, away from light

INACTIVE INGREDIENT

Inactive Ingredients Alcohol USP, FD&C Red Dye #40, Lavender Oil NF, Lemon Oil NF, Nutmeg Oil NF, Purified Water USP

QUESTIONS

Questions 1.800.835.2263

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FIRST AID ONLY AMMONIA INHALANTS 
ammonia inhalants inhalant

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0924-5401(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
LEMON OIL (UNII: I9GRO824LL)
WATER (UNII: 059QF0KO0R)
LAVENDER OIL (UNII: ZBP1YXW0H8)
ALCOHOL (UNII: 3K9958V90M)
FD&C RED NO. 40 (UNII: WZB9127XOA)
NUTMEG OIL (UNII: Z1CLM48948)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0924-5401-01	10 in 1 CARTON	01/01/2006
1		0.3 mL in 1 AMPULE; Type 0: Not a Combination Product
2	NDC: 0924-5401-02	100 in 1 CARTON	01/01/2006
2		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		01/01/2006

Labeler - Acme United Corporation (001180207)

Registrant - Acme United Corporation (001180207)

Establishment
Name	Address	ID/FEI	Business Operations
Acme United Corporation		045924339	relabel(0924-5401) , repack(0924-5401)

Establishment
Name	Address	ID/FEI	Business Operations
Acme United Corporation		080119599	relabel(0924-5401) , repack(0924-5401)