warnings
Warnings Sore throat warning: if sore throat is severe, persists more than 2 days, is accompanied or followed by a fever, headache, rash, nausea, or vomiting, consult a doctor promptly.
Cough and Bronchial Daytime
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
- Cough and Bronchial Daytime
- Generic name
- ACONITUM NAPELLUS, BRYONIA ALBA ROOT, CALCIUM SULFIDE, SPONGIA OFFICINALIS SKELETON, ROASTED, TIN
- Manufacturer
- Schwabe North America, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- ab0a4fd6-2311-4dd4-a146-949b86bfb4e7
- SPL ID
- 495817a1-a080-46ea-a5fb-14ca9b261fe5
- Version
- 1
- Effective date
- 2026-05-14
- Source export date
- 2026-09-28
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:26:14
| 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 | Cough and Bronchial Daytime | openfda.brand_name | |
| generic name | ACONITUM NAPELLUS, BRYONIA ALBA ROOT, CALCIUM SULFIDE, SPONGIA OFFICINALIS SKELETON, ROASTED, TIN | openfda.generic_name | |
| manufacturer name | Schwabe North America, Inc. | openfda.manufacturer_name | |
| ndc | package | 53499-1625-8 | openfda.package_ndc |
| ndc | package | 53499-1625-4 | openfda.package_ndc |
| ndc | product | 53499-1625 | openfda.product_ndc |
| ndc11 | package | 53499162504 | derived:openfda.package_ndc |
| ndc11 | package | 53499162508 | derived:openfda.package_ndc |
| spl id | 495817a1-a080-46ea-a5fb-14ca9b261fe5 | id | |
| spl set id | ab0a4fd6-2311-4dd4-a146-949b86bfb4e7 | set_id | |
| unii | 387GMG9FH5 | openfda.unii | |
| unii | T7J046YI2B | openfda.unii | |
| unii | U0NQ8555JD | openfda.unii | |
| unii | 1PIP394IID | openfda.unii | |
| unii | 1MBW07J51Q | 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.