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-52
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-52
- Generic name
- AETHUSA CYNAPIUM, APOMORPHINE HYDROCHLORIDE, ANAMIRTA COCCULUS SEED, COLCHICUM AUTUMNALE BULB, IPECAC, STRYCHNOS NUX-VOMICA SEED, VERATRUM ALBUM ROOT, AND KEROSENE
- Manufacturer
- DNA Labs, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- d454b66a-c55c-4082-b7c4-a90f43d2d442
- SPL ID
- 2b9ec8dd-73aa-e366-e063-6394a90ae792
- 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 05:26:34
| 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-52 | openfda.brand_name | |
| generic name | AETHUSA CYNAPIUM, APOMORPHINE HYDROCHLORIDE, ANAMIRTA COCCULUS SEED, COLCHICUM AUTUMNALE BULB, IPECAC, STRYCHNOS NUX-VOMICA SEED, VERATRUM ALBUM ROOT, AND KEROSENE | openfda.generic_name | |
| manufacturer name | DNA Labs, Inc. | openfda.manufacturer_name | |
| ndc | package | 58264-0052-1 | openfda.package_ndc |
| ndc | product | 58264-0052 | openfda.product_ndc |
| ndc11 | package | 58264005201 | derived:openfda.package_ndc |
| spl id | 2b9ec8dd-73aa-e366-e063-6394a90ae792 | id | |
| spl set id | d454b66a-c55c-4082-b7c4-a90f43d2d442 | set_id | |
| unii | 269XH13919 | openfda.unii | |
| unii | 993QHL78E6 | openfda.unii | |
| unii | F39049Y068 | openfda.unii | |
| unii | M6936L953C | openfda.unii | |
| unii | 62I3C8233L | openfda.unii | |
| unii | 810258W28U | openfda.unii | |
| unii | QNS6W5US1Z | openfda.unii | |
| unii | 1C89KKC04E | 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.