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 2%

PURPOSE

Inhalant

INDICATIONS & USAGE

For the temporarystimulation ofthe senses to restore alertness.

WARNINGS

For inHalAtion use only.
Avoid direct contact with eyes.lfcontact occurs,rinse thoroughly with water fori5 minutes.Use only as directed. Misuse may be harmful.
Use in a well-ventilated area.Do notuse in enclosedspaces
Prolonged exposure maycause irritation.Discantinue useifdiscomfort occurs.
Possible side effectsinclude nasallritation,coughing.or shortness of breath.lfsymptoms persist, discontinue use and consulta doctor

DO NOT USE

Do not ingest or apply to skin.

WHEN USING

Avoid contact with eyes,ears, and mouth.

Ifproduct gets into eyes, rinse thoroughly with water for 15minutes.
Stop use and ask a doctorifirritation orrash occurs.
These may be signs ofaserious condition.

STOP USE

Stop use and ask a doctorifirritation or rash occurs.
These may be signs ofa serious condition.

KEEP OUT OF REACH OF CHILDREN

Keep outofreach ofchildren.lfswallowed,get medical
help or contacta Poison control center immediately at 1-800-222-1222.

DOSAGE & ADMINISTRATION

INACTIVE INGREDIENT

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: 85765-002
Route of Administration	RESPIRATORY (INHALATION)

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMMONIA (UNII: 5138Q19F1X) (AMMONIA - UNII:5138Q19F1X)	AMMONIA	2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
PEPPERMINT OIL (UNII: AV092KU4JH)
COTTON (UNII: 70LDW53ROO)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85765-002-01	1 in 1 BOX	06/25/2025
1		53 g in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		06/25/2025

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

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Ze'ai Electronic Co., Ltd.		698455780	manufacture(85765-002)