SMELLING SALTS- ammonia granule

Smelling Salts by

Drug Labeling and Warnings

Smelling Salts by is a Otc medication manufactured, distributed, or labeled by Shenzhen Finona Information Technology Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ammonia 15%

PURPOSE

Inhalant

INDICATIONS & USAGE

For the temporary stimulation of the senses to restore alertness.

WARNINGS

For inhalation use only.

Do not ingest or apply to skin.
Avoid direct contact with eyes. lf contact occurs, rinsethoroughly with water for 15 minutes.
Use only as directed. Misuse may be harmful.
Use in a well-ventilated area. Do not use in enclosed spaces.
Prolonged exposure may cause irritation, Discontinue use if discomfort occurs.
Possible side effects include nasal irritation, coughing, or shortness of breath. lf symptoms persist, discontinue use and consult a doctor.

DO NOT USE

It you have respiratory conditions such as asthma oremphysema.
If you have heart disease or high blood pressure.
If you are allergic to ammonia or strong odors.

WHEN USING

Avoid contact with eyes, ears, and mouth.
lf product gets into eyes, rinse thoroughly with water for 15 minutes.
Stop use and ask a doctor ifirritation or rash occurs.
These may be signs of a serious condition.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. lfswallowed, get medical
help or contact a Poison Control centerimmediately at
1-800-222-1222

DOSAGE & ADMINISTRATION

Hold bottle 10-15 cm (4-6 inches) from nostrils.
Inhale gently. Do not place directly inside the nostrils.
Do not inhale for more than 2 seconds per use.
Do not use more than once every 60 minutes.
Do not use more than 10 times per day.
Use only as needed. lfsymptoms persist, consult ahealthcare professional

INACTIVE INGREDIENT

Alcohol
Cotton
Peppermint Oil

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SMELLING SALTS 
ammonia granule

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85839-005
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)
COTTON (UNII: 70LDW53ROO)
PEPPERMINT OIL (UNII: AV092KU4JH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85839-005-01	30 g in 1 BOTTLE; Type 0: Not a Combination Product	06/26/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		06/26/2025

Labeler - Shenzhen Finona Information Technology Co., Ltd (511271543)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Finona Information Technology Co., Ltd		511271543	manufacture(85839-005)