warnings
Warnings Use only if cap seal is unbroken. If pregnant or breastfeeding, ask a healthcare professional before use. Keep this and all medication out of the reach of children.
D-42
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
- D-42
- Generic name
- HORSE CHESTNUT, ATROPA BELLADONNA, CALCIUM FLUORIDE, MILK THISTLE, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, DAPHNE MEZEREUM BARK, ANEMONE PRATENSIS, CLAVICEPS PURPUREA SCLEROTIUM, VIPERA BERUS VENOM, AND BOS TAURUS PLACENTA
- Manufacturer
- DNA Labs, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 400cbb19-5475-43ee-8630-608e673dc986
- SPL ID
- 2b9ea788-da08-c3ef-e063-6394a90a6b11
- Version
- 3
- Effective date
- 2025-01-13
- Source export date
- 2026-10-27
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/b7a5e61d87a3b8f87f4c3ff7b526bfbf6baf84c840f565574c7d83d4083e2b38/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:50:18
| Harmonized routes |
|---|
| SUBLINGUAL |
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 | D-42 | openfda.brand_name | |
| generic name | HORSE CHESTNUT, ATROPA BELLADONNA, CALCIUM FLUORIDE, MILK THISTLE, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, DAPHNE MEZEREUM BARK, ANEMONE PRATENSIS, CLAVICEPS PURPUREA SCLEROTIUM, VIPERA BERUS VENOM, AND BOS TAURUS PLACENTA | openfda.generic_name | |
| manufacturer name | DNA Labs, Inc. | openfda.manufacturer_name | |
| ndc | package | 58264-0042-1 | openfda.package_ndc |
| ndc | product | 58264-0042 | openfda.product_ndc |
| ndc11 | package | 58264004201 | derived:openfda.package_ndc |
| spl id | 2b9ea788-da08-c3ef-e063-6394a90a6b11 | id | |
| spl set id | 400cbb19-5475-43ee-8630-608e673dc986 | set_id | |
| unii | O3B55K4YKI | openfda.unii | |
| unii | X2N6E405GV | openfda.unii | |
| unii | 3C18L6RJAZ | openfda.unii | |
| unii | U946SH95EE | openfda.unii | |
| unii | 0ORO6NCA4M | openfda.unii | |
| unii | 8E272251DI | openfda.unii | |
| unii | WQZ3G9PF0H | openfda.unii | |
| unii | 01G9XEA93N | openfda.unii | |
| unii | T7S323PKJS | openfda.unii | |
| unii | 83AL37E3A7 | 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.