QUALITY CHOICE AROMATIC AMMONIA SPIRIT- ammonia 2% liquid

Quality Choice Aromatic Ammonia Spirit by

Drug Labeling and Warnings

Quality Choice Aromatic Ammonia Spirit by is a Otc medication manufactured, distributed, or labeled by Chain Drug Market Association, Humco Holding Group, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

WARNINGS AND PRECAUTIONS

 Drug Facts

Active Ingredient

 Ammonia 2 %

Purpose

 Respiratory Stimulant

Indication

Respiratory stimulant used as a smelling salts to treat or prevent fainting.

Warnings

 For external use only. Avoid eye contact with liquid vapors. Avoid inhaling more than a slight whiff. May cause irritation if excess is inhaled.

If pregnant or nursing a baby

 seek the advice of a doctor before using this product.

Keep out of the reach of children

 In case of accidental ingestion, seek professional assistance or contact a Poison Control Center right away.

Directions

 Inhale a slight whiff to treat a "faining spell"

Inactive Ingredients

 Ammonium Carbonate, Ethyl Alcohol 656%, Lavender Oil, Lemon Oil Terpenless, Myristica Oil and Purified Water.

Other Information

 Flammable: Keep away from spark, heat or flame. Keep tightly closed at room temperature not toexceed 30C (86F).

Label

INGREDIENTS AND APPEARANCE

QUALITY CHOICE AROMATIC AMMONIA SPIRIT 
ammonia 2% liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63868-489
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMMONIA (UNII: 5138Q19F1X) (AMMONIA - UNII:5138Q19F1X)	AMMONIA	20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
AMMONIUM CARBONATE (UNII: NJ5VT0FKLJ)
ALCOHOL (UNII: 3K9958V90M)
LAVENDER OIL (UNII: ZBP1YXW0H8)
LEMON OIL, TERPENELESS (UNII: X69W83NI7V)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63868-489-02	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/12/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		01/01/2008

Labeler - Chain Drug Market Association (011920774)

Registrant - Humco Holding Group, Inc. (825672884)

Establishment
Name	Address	ID/FEI	Business Operations
Humco Holding Group, Inc.		825672884	manufacture(63868-489) , analysis(63868-489) , pack(63868-489) , label(63868-489)