warnings
Warnings For external use only. Do not use if you have breathing problems such as asthma or emphysema. Stop use and ask a doctor if condition persists.
ammonia inhalants
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- ammonia inhalants
- Generic name
- INHALANT
- Manufacturer
- Epic Medical Supply Corp
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 20e849e5-8517-b9fd-e063-6394a90a0d23
- SPL ID
- 20e849e5-8518-b9fd-e063-6394a90a0d23
- Version
- 1
- Effective date
- 2024-09-03
- Source export date
- 2026-10-30
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/a3e33fe073aa0aa94eb690c6684c74434c63cebfbf7c5530205a2c3e957ecb8b/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:38:50
| Harmonized routes |
|---|
| RESPIRATORY (INHALATION) |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| brand name | ammonia inhalants | openfda.brand_name | |
| generic name | INHALANT | openfda.generic_name | |
| manufacturer name | Epic Medical Supply Corp | openfda.manufacturer_name | |
| ndc | package | 82749-150-01 | openfda.package_ndc |
| ndc | package | 82749-150-02 | openfda.package_ndc |
| ndc | product | 82749-150 | openfda.product_ndc |
| ndc11 | package | 82749015002 | derived:openfda.package_ndc |
| ndc11 | package | 82749015001 | derived:openfda.package_ndc |
| rxcui | 1299889 | openfda.rxcui | |
| spl id | 20e849e5-8518-b9fd-e063-6394a90a0d23 | id | |
| spl set id | 20e849e5-8517-b9fd-e063-6394a90a0d23 | set_id | |
| unii | 5138Q19F1X | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.