warnings
Consult a physician for use in children under 6 years of age. Contact a doctor if symptoms persist.
Comfort Down There Hemorrhoids
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
- Comfort Down There Hemorrhoids
- Generic name
- AESCULUS HIPPOCASTANUM 5C, ALOE 5C, BERBERIS VULGARIS 3C, CAPSICUM ANNUUM 5C, CARDUUS MARIANUS 3C, NUX VOMICA 5C, PULSATILLA 9C
- Manufacturer
- SEVENE USA
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 55001764-8bc9-cbac-e063-6394a90a455c
- SPL ID
- 594f5100-8657-45a9-e063-6394a90a3ce5
- Version
- 3
- Effective date
- 2026-08-18
- Source export date
- 2026-10-30
- 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/2026-10-30/9dea423b9e87a781c152bc6e136923fb91acb0732a7a0ec0d2a51142148f160c/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 18:44:09
| 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 | Comfort Down There Hemorrhoids | openfda.brand_name | |
| generic name | AESCULUS HIPPOCASTANUM 5C, ALOE 5C, BERBERIS VULGARIS 3C, CAPSICUM ANNUUM 5C, CARDUUS MARIANUS 3C, NUX VOMICA 5C, PULSATILLA 9C | openfda.generic_name | |
| manufacturer name | SEVENE USA | openfda.manufacturer_name | |
| ndc | package | 76472-7009-1 | openfda.package_ndc |
| ndc | package | 76472-7009-2 | openfda.package_ndc |
| ndc | product | 76472-7009 | openfda.product_ndc |
| ndc11 | package | 76472700901 | derived:openfda.package_ndc |
| ndc11 | package | 76472700902 | derived:openfda.package_ndc |
| spl id | 594f5100-8657-45a9-e063-6394a90a3ce5 | id | |
| spl set id | 55001764-8bc9-cbac-e063-6394a90a455c | set_id | |
| unii | 269XH13919 | openfda.unii | |
| unii | 1TH8Q20J0U | openfda.unii | |
| unii | U946SH95EE | openfda.unii | |
| unii | 7FKZ3QQQ1F | openfda.unii | |
| unii | 2331W47PSX | openfda.unii | |
| unii | R0RP86FLN8 | 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.