warnings
Warnings Stop use and consult a doctor if symptoms worsen or persist for more than 7 days. If pregnant or breast-feeding , ask a healthcare professional before use.
Lungs and Bronchial Relief
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
- Lungs and Bronchial Relief
- Generic name
- AMMONIUM CARBONICUM, ANTIMONIUM ARSENICICUM, ANTIMONIUM TARTARICUM, ARSENICUM ALBUM, BROMIUM, CARBO VEGETABILIS, CHLORINUM, KALI CARBONICUM, LOBELIA INFLATA, STANNUM METALLICUM, SULPHURICUM ACIDUM.
- Manufacturer
- King Bio Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- fc4d4a56-3483-4cae-9818-fdae4e95ec6c
- SPL ID
- e3a1f7b0-12dd-49c1-9d0c-6b74fe7ead4e
- Version
- 2
- Effective date
- 2026-03-02
- Source export date
- 2026-10-12
- 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/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:57:16
| Harmonized routes |
|---|
| ORAL |
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 | Lungs and Bronchial Relief | openfda.brand_name | |
| generic name | AMMONIUM CARBONICUM, ANTIMONIUM ARSENICICUM, ANTIMONIUM TARTARICUM, ARSENICUM ALBUM, BROMIUM, CARBO VEGETABILIS, CHLORINUM, KALI CARBONICUM, LOBELIA INFLATA, STANNUM METALLICUM, SULPHURICUM ACIDUM. | openfda.generic_name | |
| manufacturer name | King Bio Inc. | openfda.manufacturer_name | |
| ndc | package | 57955-9991-2 | openfda.package_ndc |
| ndc | product | 57955-9991 | openfda.product_ndc |
| ndc11 | package | 57955999102 | derived:openfda.package_ndc |
| spl id | e3a1f7b0-12dd-49c1-9d0c-6b74fe7ead4e | id | |
| spl set id | fc4d4a56-3483-4cae-9818-fdae4e95ec6c | set_id | |
| unii | 2P3VWU3H10 | openfda.unii | |
| unii | 387GMG9FH5 | openfda.unii | |
| unii | 9PP1T3TC5U | openfda.unii | |
| unii | SBV4XY874G | openfda.unii | |
| unii | WE3458XNFT | openfda.unii | |
| unii | 4R7X1O2820 | openfda.unii | |
| unii | NJ5VT0FKLJ | openfda.unii | |
| unii | DL6OZ476V3 | openfda.unii | |
| unii | BQN1B9B9HA | openfda.unii | |
| unii | S7V92P67HO | openfda.unii | |
| unii | O40UQP6WCF | 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.