SMELLING SALTS- ammonia powder

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 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. lfcontact 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 useif discomfort occurs.
Possible side effects include nasal imitation, coughing, orshortness ofbreath. lfsymptoms persist, discontinue useand consult a doctor.

DO NOT USE

lf you have respiratory conditions such as asthma oremphysema.
lf you have heart disease or high blood pressure.
If you are allergic to ammonia orstrong 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 if irritation or rash occurs.
These may be signs of a serious condition.

STOP USE

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 ofreach ofchildren.lfswallowed, get medical
help or contact a Poison Control Center immediately 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 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 ahealthcare professional!

INACTIVE INGREDIENT

aromatic
solvent
Alcohol
Cotton
Peppermint Oil

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SMELLING SALTS 
ammonia powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85765-001
Route of Administration	INTRASINAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMMONIA (UNII: 5138Q19F1X) (AMMONIA - UNII:5138Q19F1X)	AMMONIA	15 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
AROMATIC-L-AMINO-ACID DECARBOXYLASE (UNII: BY6OQ7Q6TP)
SOLVENT BLUE 102 (UNII: 88R726QBG3)
ALCOHOL (UNII: 3K9958V90M)
COTTON (UNII: 70LDW53ROO)
PEPPERMINT OIL (UNII: AV092KU4JH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85765-001-01	30 g in 1 BOTTLE; Type 0: Not a Combination Product	06/05/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	06/05/2025

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

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Ze'ai Electronic Co., Ltd.		698455780	manufacture(85765-001)