smelling salts

Manufacturer
Shenzhen Ze'ai Electronic Co., Ltd.
Effective date
2025-09-10
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:13:28

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

Forthe temporarystimulation of the senses to restore alertness

WARNINGS SECTION


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.

OTC - DO NOT USE SECTION


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.

OTC - WHEN USING SECTION


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.

OTC - STOP USE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION


Keep out ofreach ofchildren.lfswallowed, get medical
help or contacta Poison Control Centerimmediately at 1-800-222-1222

DOSAGE & ADMINISTRATION SECTION


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 SECTION

Alcohol
Cotton
Peppermint Oil

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1299889ammonia 15 % Nasal InhalantPSN4
1299889ammonia 150 MG/ML Nasal InhalantSCD4
1299889ammonia 0.045 GM per 0.3 ML Nasal InhalantSY4
1299889ammonia 0.3 ML Nasal InhalantSY4
1299889ammonia 15 % Nasal InhalantSY4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85765-003-01smelling salts50 g in 1 BOTTLEINHALANT504

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85765-00385765-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
COTTON70LDW53ROOIACT
PEPPERMINT OILAV092KU4JHIACT
AMMONIA5138Q19F1XACTIB

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
3e7d9782-4551-9f08-e063-6294a90a4f3538c57576-e2c1-c447-e063-6394a90a62ae2025-09-10WarningsExact identifier
spl id: 3e7d9782-4551-9f08-e063-6294a90a4f35
spl set id: 38c57576-e2c1-c447-e063-6394a90a62ae

Reported adverse events (FAERS/openFDA)#

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