smelling salts

Manufacturer
Shenzhen Ze'ai Electronic Co., Ltd.
Effective date
2025-06-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:02:17

Label at a glance#

Productsmelling salts
Active ingredientAMMONIA
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ammonia 15%

OTC - PURPOSE SECTION

Inhalant

INDICATIONS & USAGE SECTION

For the temporary stimulation of the senses to restore alertness.

WARNINGS SECTION


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.

OTC - DO NOT USE SECTION


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.

OTC - WHEN USING SECTION


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.

OTC - STOP USE SECTION

Stop use and ask a doctor ifirritation or rash occurs.
These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out ofreach ofchildren.lfswallowed, get medical
help or contact a Poison Control Center immediately at
1-800-222-1222

DOSAGE & ADMINISTRATION SECTION


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 SECTION

aromatic
solvent
Alcohol
Cotton
Peppermint Oil

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1299889ammonia 15 % Nasal InhalantPSN2
1299889ammonia 150 MG/ML Nasal InhalantSCD2
1299889ammonia 0.045 GM per 0.3 ML Nasal InhalantSY2
1299889ammonia 0.3 ML Nasal InhalantSY2
1299889ammonia 15 % Nasal InhalantSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85765-001-01smelling salts30 g in 1 BOTTLEPOWDER302

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85765-00185765-001-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
36d08534-ac8d-5152-e063-6294a90ae12936ceef42-c3ea-7302-e063-6394a90a94da2025-06-05WarningsExact identifier
spl id: 36d08534-ac8d-5152-e063-6294a90ae129
spl set id: 36ceef42-c3ea-7302-e063-6394a90a94da

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.