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-49
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-49
- Generic name
- ARSENIC TRIOXIDE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, MERCURIC SULFIDE, POTASSIUM DICHROMATE, MERCURIUS SOLUBILIS, ANEMONE PRATENSIS, SEPIA OFFICINALIS JUICE, AND SULFUR
- Manufacturer
- DNA Labs, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 26800b04-81c7-4094-afe8-4db6ca878f6d
- SPL ID
- 2b9ec8dd-73af-e366-e063-6394a90ae792
- Version
- 3
- Effective date
- 2025-01-13
- Source export date
- 2026-10-23
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-23/a51739e93506c2ea49960d9d8b93613806ce6897e579b6294cbc5a7a56cff555/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- 003b0607e7bf4d3ce17ccc0942e221303b4f62b17a6a00c54547eda454293380
- Import run
- 20261026T035824Z
- Imported at
- 2026-10-26 04:14:04
| 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-49 | openfda.brand_name | |
| generic name | ARSENIC TRIOXIDE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, MERCURIC SULFIDE, POTASSIUM DICHROMATE, MERCURIUS SOLUBILIS, ANEMONE PRATENSIS, SEPIA OFFICINALIS JUICE, AND SULFUR | openfda.generic_name | |
| manufacturer name | DNA Labs, Inc. | openfda.manufacturer_name | |
| ndc | package | 58264-0049-1 | openfda.package_ndc |
| ndc | product | 58264-0049 | openfda.product_ndc |
| ndc11 | package | 58264004901 | derived:openfda.package_ndc |
| spl id | 2b9ec8dd-73af-e366-e063-6394a90ae792 | id | |
| spl set id | 26800b04-81c7-4094-afe8-4db6ca878f6d | set_id | |
| unii | 324Y4038G2 | openfda.unii | |
| unii | QDL83WN8C2 | openfda.unii | |
| unii | 2E32821G6I | openfda.unii | |
| unii | S7V92P67HO | openfda.unii | |
| unii | 8E272251DI | openfda.unii | |
| unii | 70FD1KFU70 | openfda.unii | |
| unii | T4423S18FM | openfda.unii | |
| unii | ZI0T668SF1 | 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.