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 Nighttime
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 Nighttime
- Generic name
- ACONITUM NAPELLUS, ALFALFA, ARABICA COFFEE BEAN, MEDICAGO SATIVA LEAF, BRYONIA ROOT, CALCIUM CATION, SPONGIA OFFICINALIS SKELETON, ROASTED, TIN
- Manufacturer
- Schwabe North America, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 31445469-8f7f-4729-8128-fc53d5e5ab06
- SPL ID
- 01b5e098-5ae0-4462-bfb7-d56e9d1d9fd9
- Version
- 1
- Effective date
- 2026-07-22
- Source export date
- 2026-10-12
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:46:37
| 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 Nighttime | openfda.brand_name | |
| generic name | ACONITUM NAPELLUS, ALFALFA, ARABICA COFFEE BEAN, MEDICAGO SATIVA LEAF, BRYONIA ROOT, CALCIUM CATION, SPONGIA OFFICINALIS SKELETON, ROASTED, TIN | openfda.generic_name | |
| manufacturer name | Schwabe North America, Inc. | openfda.manufacturer_name | |
| ndc | package | 53499-1627-8 | openfda.package_ndc |
| ndc | package | 53499-1627-4 | openfda.package_ndc |
| ndc | product | 53499-1627 | openfda.product_ndc |
| ndc11 | package | 53499162708 | derived:openfda.package_ndc |
| ndc11 | package | 53499162704 | derived:openfda.package_ndc |
| spl id | 01b5e098-5ae0-4462-bfb7-d56e9d1d9fd9 | id | |
| spl set id | 31445469-8f7f-4729-8128-fc53d5e5ab06 | set_id | |
| unii | 387GMG9FH5 | openfda.unii | |
| unii | 3SW678MX72 | openfda.unii | |
| unii | DJO934BRBD | openfda.unii | |
| unii | HY3L927V6M | 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.