SMELLING SALTS- ammonia inhalant

smelling salts by

Drug Labeling and Warnings

smelling salts by is a Otc medication manufactured, distributed, or labeled by Shenzhen Ze'ai Electronic Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ammonia 2%

PURPOSE

Inhalant

INDICATIONS & USAGE

Forthe temporarystimulation of the senses to restore alertness

WARNINGS

ForinHalAtion use only.
Do notingest or apply to skin.
Avoid direct contact with eyes. lfcontact occurs, rinse thoroughly with water for l5 minutes.
Use only as directed. Misuse may be harmful.
Use in a well-ventilated area. Donot usein enclosed spaces.
Prolonged exposure may cause irritation. Discontinue use if discomfort occurs.
Possible side effectsinclude nasaliritation, coughing, or shortness of breath.lf symptoms persist, discontinue use and consult a doctor.

DO NOT USE

lf you have respiratory conditions such as asthma oremphysemA.
lf you have heart disease or high blood pressure.
lf you are allergic to ammonia or strongodors.

WHEN USING

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

STOP USE

Stop use and ask a doctorifirritation orrash occursThese may be signs of a serious condition,

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

Keep out ofreach ofchildren.lfswallowed, get medical
help or contacta 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 directlyinside the nostrils.
Do notinhale 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 a healthcare professional.

INACTIVE INGREDIENT

Alcohol
Cotton
Peppermint Oil

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SMELLING SALTS 
ammonia inhalant

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85765-003
Route of Administration	RESPIRATORY (INHALATION)

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMMONIA (UNII: 5138Q19F1X) (AMMONIA - UNII:5138Q19F1X)	AMMONIA	0.02 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: 85765-003-01	50 g in 1 BOTTLE; Type 0: Not a Combination Product	06/30/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M011	06/30/2025

Labeler - Shenzhen Ze'ai Electronic Co., Ltd. (698455780)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Ze'ai Electronic Co., Ltd.		698455780	manufacture(85765-003)