warnings
WARNINGS Consult a physician for use in children under 6 years of age. Contact a doctor if symptoms persist.
Cold Comfort Cold and Cough
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
- Cold Comfort Cold and Cough
- Generic name
- ALLIUM CEPA 5C, EUPHRASIA OFFICINALIS 5C, HYDRASTIS CANADENSIS 5C, NUX VOMICA 5C, PULSATILLA 5C, RUMEX CRISPUS 5C,SABADILLA 5C, SAMBUCUS NIGRA 5C
- Manufacturer
- SEVENE USA
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 54e9282a-604d-4acd-e063-6394a90a59ff
- SPL ID
- 594f5d57-799c-8ef0-e063-6294a90a1761
- Version
- 3
- Effective date
- 2026-08-18
- Source export date
- 2026-10-12
- Source partition
- 14
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/acb9b4700b9af1bdda1c389c7b35bfe38fd6d1a62aa48d17832812be4029b84f/drug-label-0014-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 03:13:36
| Harmonized routes |
|---|
| BUCCAL |
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 | Cold Comfort Cold and Cough | openfda.brand_name | |
| generic name | ALLIUM CEPA 5C, EUPHRASIA OFFICINALIS 5C, HYDRASTIS CANADENSIS 5C, NUX VOMICA 5C, PULSATILLA 5C, RUMEX CRISPUS 5C,SABADILLA 5C, SAMBUCUS NIGRA 5C | openfda.generic_name | |
| manufacturer name | SEVENE USA | openfda.manufacturer_name | |
| ndc | package | 76472-7003-2 | openfda.package_ndc |
| ndc | package | 76472-7003-1 | openfda.package_ndc |
| ndc | product | 76472-7003 | openfda.product_ndc |
| ndc11 | package | 76472700301 | derived:openfda.package_ndc |
| ndc11 | package | 76472700302 | derived:openfda.package_ndc |
| spl id | 594f5d57-799c-8ef0-e063-6294a90a1761 | id | |
| spl set id | 54e9282a-604d-4acd-e063-6394a90a59ff | set_id | |
| unii | 269XH13919 | openfda.unii | |
| unii | 8P2VLG2456 | openfda.unii | |
| unii | R763EBH88T | openfda.unii | |
| unii | L4W0HL3P0F | openfda.unii | |
| unii | 9N1RM2S62C | openfda.unii | |
| unii | 6NAF1689IO | openfda.unii | |
| unii | CT03BSA18U | openfda.unii | |
| unii | I76KB35JEV | 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.