Smelling Salt

Manufacturer
Nanning Xingshuang Network Technology Studio (A Sole Proprietorship)
Effective date
2025-08-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:09:39

Label at a glance#

ProductSmelling Salt
Active ingredientAMMONIUM CARBONATE
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ammonium Carbonate 15%

OTC - PURPOSE SECTION

Inhalant

INDICATIONS & USAGE SECTION

Uses:To prevent or treat fainting

WARNINGS SECTION


Avoid contact with skin or eyes. Rinse immediately with water for 15 minutes ifexposed.
Flammable. Keep away from heat, fames, or sparks.
For emergency use only. Not a substitute for professional medica!

OTC - DO NOT USE SECTION

1.Individuals with asthma or chronic respiratory conditions
2.Children under 2 years ofage.

OTC - WHEN USING SECTION

Avoid repeated inhalation. Do not use more than 2 times perapplication.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION


OTC- Keep Out ofReach OfChildren:Store in a cool, dry place inaccessible to children.
Swallowing may cause poisoning.

DOSAGE & ADMINISTRATION SECTION

Directions:1.Hold bottle 10-15 cm from nostrils and inhale slowly 1-2 times2. Seal tightly after each use to prevent prolonged exposure.

INACTIVE INGREDIENT SECTION

Cotton
Peppermint Flavour

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label1label1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1299889ammonia 15 % Nasal InhalantPSN1
1299889ammonia 150 MG/ML Nasal InhalantSCD1
1299889ammonia 0.045 GM per 0.3 ML Nasal InhalantSY1
1299889ammonia 0.3 ML Nasal InhalantSY1
1299889ammonia 15 % Nasal InhalantSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85999-001-01Smelling Salt30 g in 1 BOTTLELIQUID301

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
85999-00185999-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
AMMONIUM CARBONATENJ5VT0FKLJACTIB
COTTON70LDW53ROOIACT
PEPPERMINTV95R5KMY2BIACT

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
3bbdb3a8-d0aa-cb90-e063-6394a90a41e03bbdb3a8-d0a9-cb90-e063-6394a90a41e02025-08-06WarningsExact identifier
spl id: 3bbdb3a8-d0aa-cb90-e063-6394a90a41e0
spl set id: 3bbdb3a8-d0a9-cb90-e063-6394a90a41e0

Reported adverse events (FAERS/openFDA)#

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