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, c onsult a doctor promptly.
Cough and Bronchial Daytime Syrup
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 Syrup
- Generic name
- ACONITUM NAPELLUS, BRYONIA ALBA ROOT, CALCIUM CATION, SPONGIA OFFICINALIS SKELETON, ROASTED, TIN
- Manufacturer
- Schwabe Mexico, S.A. de C.V.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- e8949f67-1b05-40a2-96a5-d4d1124915ff
- SPL ID
- 3bc70af5-fff0-4ff5-887c-41425e7d6911
- Version
- 6
- Effective date
- 2026-10-22
- Source export date
- 2026-10-30
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/0b630a6825fc0c8abba22d7c8fd4d069bde78bef928766047ddbb369119f337f/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:00:56
| 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 Syrup | openfda.brand_name | |
| generic name | ACONITUM NAPELLUS, BRYONIA ALBA ROOT, CALCIUM CATION, SPONGIA OFFICINALIS SKELETON, ROASTED, TIN | openfda.generic_name | |
| manufacturer name | Schwabe Mexico, S.A. de C.V. | openfda.manufacturer_name | |
| ndc | package | 68466-1008-9 | openfda.package_ndc |
| ndc | package | 68466-1008-4 | openfda.package_ndc |
| ndc | product | 68466-1008 | openfda.product_ndc |
| ndc11 | package | 68466100804 | derived:openfda.package_ndc |
| ndc11 | package | 68466100809 | derived:openfda.package_ndc |
| spl id | 3bc70af5-fff0-4ff5-887c-41425e7d6911 | id | |
| spl set id | e8949f67-1b05-40a2-96a5-d4d1124915ff | 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.