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
- 8d2e612c-6da0-48f5-ae5f-b377939f6009
- Version
- 5
- Effective date
- 2025-12-08
- Source export date
- 2026-10-12
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:12:39
| 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 | 8d2e612c-6da0-48f5-ae5f-b377939f6009 | 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.