FDA.reportPublic FDA data

Hyvia Ammonia Inhalant

Manufacturer
Hyvia Health LLC
Effective date
2025-12-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:34:03

Label at a glance#

ProductHyvia Ammonia Inhalant
Active ingredientAMMONIUM CHLORIDE, SODIUM CARBONATE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ammonium Chloride 333 mg
Sodium Carbonate Monohydrate 667 mg

OTC - PURPOSE SECTION

Respiratory stimulant

INDICATIONS & USAGE SECTION

Temporarily relieves nasal congestion.

WARNINGS SECTION

For external use only.
Do not ingest.
If symptoms persist, consult a healthcare professional.

DOSAGE & ADMINISTRATION SECTION

Inhale vapors as needed.
Use only as directed.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

INACTIVE INGREDIENT SECTION

Water

BEST SMELLING SALTS

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BEST SMELLING SALTSBEST SMELLING SALTS

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87331-00387331-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
AMMONIUM CHLORIDE01Q9PC255DACTIM
SODIUM CARBONATE45P3261C7TACTIB

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
4c5ea288-bb71-8d10-e063-6294a90a6f4246a86134-c911-ca34-e063-6294a90a5de02026-03-06WarningsExact identifier
spl set id: 46a86134-c911-ca34-e063-6294a90a5de0

Reported adverse events (FAERS/openFDA)#

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