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-37
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-37
- Generic name
- ALUMINUM OXIDE, BRYONIA ALBA ROOT, CITRULLUS COLOCYNTHIS FRUIT PULP, LACHESIS MUTA VENOM, LYCOPODIUM CLAVATUM SPORE, MERCURIC CHLORIDE, STRYCHNOS NUX-VOMICA SEED, LEAD ACETATE ANHYDROUS, AND SULFUR
- Manufacturer
- DNA Labs, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 3b408532-b84b-4398-ab8d-64d5a9c8d092
- SPL ID
- 2b9ec82d-e5f6-ae16-e063-6394a90a5559
- Version
- 3
- Effective date
- 2025-01-13
- Source export date
- 2026-09-28
- 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/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:27:10
| 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-37 | openfda.brand_name | |
| generic name | ALUMINUM OXIDE, BRYONIA ALBA ROOT, CITRULLUS COLOCYNTHIS FRUIT PULP, LACHESIS MUTA VENOM, LYCOPODIUM CLAVATUM SPORE, MERCURIC CHLORIDE, STRYCHNOS NUX-VOMICA SEED, LEAD ACETATE ANHYDROUS, AND SULFUR | openfda.generic_name | |
| manufacturer name | DNA Labs, Inc. | openfda.manufacturer_name | |
| ndc | package | 58264-0037-1 | openfda.package_ndc |
| ndc | product | 58264-0037 | openfda.product_ndc |
| ndc11 | package | 58264003701 | derived:openfda.package_ndc |
| spl id | 2b9ec82d-e5f6-ae16-e063-6394a90a5559 | id | |
| spl set id | 3b408532-b84b-4398-ab8d-64d5a9c8d092 | set_id | |
| unii | LMI26O6933 | openfda.unii | |
| unii | 269XH13919 | openfda.unii | |
| unii | KL498O6790 | openfda.unii | |
| unii | 53GH7MZT1R | openfda.unii | |
| unii | T7J046YI2B | openfda.unii | |
| unii | 70FD1KFU70 | openfda.unii | |
| unii | VSW71SS07I | openfda.unii | |
| unii | C88X29Y479 | openfda.unii | |
| unii | 23H32AOH17 | 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.