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 Relief ACONITUM NAPELLUS, BRYONIA ALBA ROOT, CALCIUM SULFIDE, SPONGIA OFFICINALIS SKELETON, ROASTED , TIN, PELARGONIUM SIDOIDES ROOT
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 Relief ACONITUM NAPELLUS, BRYONIA ALBA ROOT, CALCIUM SULFIDE, SPONGIA OFFICINALIS SKELETON, ROASTED , TIN, PELARGONIUM SIDOIDES ROOT
- Generic name
- COUGH RELIEF
- Manufacturer
- Schwabe North America, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- a95610e3-774b-4745-a2a4-fc3ba51ab4c5
- SPL ID
- a7c5f6a5-ce84-467a-aca0-866d1373a9a9
- Version
- 4
- Effective date
- 2026-03-06
- Source export date
- 2026-11-06
- 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/2026-11-06/b00a73f24c6ff050408c570063640e3d80d1f71dfc9a165d1cf072a25659445a/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 07:04:44
| 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 Relief ACONITUM NAPELLUS, BRYONIA ALBA ROOT, CALCIUM SULFIDE, SPONGIA OFFICINALIS SKELETON, ROASTED , TIN, PELARGONIUM SIDOIDES ROOT | openfda.brand_name | |
| generic name | COUGH RELIEF | openfda.generic_name | |
| manufacturer name | Schwabe North America, Inc. | openfda.manufacturer_name | |
| ndc | package | 53499-6864-4 | openfda.package_ndc |
| ndc | product | 53499-6864 | openfda.product_ndc |
| ndc11 | package | 53499686404 | derived:openfda.package_ndc |
| spl id | a7c5f6a5-ce84-467a-aca0-866d1373a9a9 | id | |
| spl set id | a95610e3-774b-4745-a2a4-fc3ba51ab4c5 | set_id | |
| unii | 387GMG9FH5 | openfda.unii | |
| unii | T7J046YI2B | openfda.unii | |
| unii | U0NQ8555JD | openfda.unii | |
| unii | 1PIP394IID | openfda.unii | |
| unii | 1MBW07J51Q | openfda.unii | |
| unii | H6J53HEX8E | 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.