warnings
WARNINGS: IF PREGNANT OR BREAST-FEEDING, ask a health professional before use. If symptoms worsen or persist for more than a week, discontinue use and contact a doctor. KEEP OUT OF REACH OF CHILDREN.
Cough Relief
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
- Generic name
- ACONITUM NAP, ANTIMON CRUD, ANTIMON SULPH, ANTIMON TART, ARALIA RAC, BRYONIA, CHELIDONIUM MAJ, CUPRUM MET, DROSERA, HEPAR SULPH CALC, KALI CARB, SPONGIA.
- Manufacturer
- OHM PHARMA INC.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 991fd747-7a46-4689-afac-381c57b91e05
- SPL ID
- d44af2b7-f773-3d27-e053-2a95a90abc46
- Version
- 4
- Effective date
- 2021-12-29
- Source export date
- 2026-09-28
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:15:23
| 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 | openfda.brand_name | |
| generic name | ACONITUM NAP, ANTIMON CRUD, ANTIMON SULPH, ANTIMON TART, ARALIA RAC, BRYONIA, CHELIDONIUM MAJ, CUPRUM MET, DROSERA, HEPAR SULPH CALC, KALI CARB, SPONGIA. | openfda.generic_name | |
| manufacturer name | OHM PHARMA INC. | openfda.manufacturer_name | |
| ndc | package | 66096-115-05 | openfda.package_ndc |
| ndc | product | 66096-115 | openfda.product_ndc |
| ndc11 | package | 66096011505 | derived:openfda.package_ndc |
| spl id | d44af2b7-f773-3d27-e053-2a95a90abc46 | id | |
| spl set id | 991fd747-7a46-4689-afac-381c57b91e05 | set_id | |
| unii | 7E889U5RNN | openfda.unii | |
| unii | 789U1901C5 | openfda.unii | |
| unii | T90W4582DU | openfda.unii | |
| unii | QR44N9XPJQ | openfda.unii | |
| unii | F79059A38U | openfda.unii | |
| unii | DL6OZ476V3 | openfda.unii | |
| unii | BQN1B9B9HA | openfda.unii | |
| unii | 1433F1I86N | 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.