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-54
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-54
- Generic name
- DIBASIC POTASSIUM PHOSPHATE, SEPIA OFFICINALIS JUICE, LYCOPODIUM CLAVATUM SPORE, PHOSPHORUS, GELSEMIUM SEMPERVIRENS ROOT, ATROPA BELLADONNA, ARSENIC TRIOXIDE, AND SEMECARPUS ANACARDIUM JUICE
- Manufacturer
- DNA Labs, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 68a206a8-6f66-4957-843c-4c4c0636e78f
- SPL ID
- 2b9ec8dd-73ab-e366-e063-6394a90ae792
- Version
- 3
- Effective date
- 2025-01-13
- Source export date
- 2026-10-27
- Source partition
- 14
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/9122bd1bdced046e8f62ea012d80757473b7d83ea1faeea61faef490e06fd630/drug-label-0014-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 21:09:46
| 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-54 | openfda.brand_name | |
| generic name | DIBASIC POTASSIUM PHOSPHATE, SEPIA OFFICINALIS JUICE, LYCOPODIUM CLAVATUM SPORE, PHOSPHORUS, GELSEMIUM SEMPERVIRENS ROOT, ATROPA BELLADONNA, ARSENIC TRIOXIDE, AND SEMECARPUS ANACARDIUM JUICE | openfda.generic_name | |
| manufacturer name | DNA Labs, Inc. | openfda.manufacturer_name | |
| ndc | package | 58264-0054-1 | openfda.package_ndc |
| ndc | product | 58264-0054 | openfda.product_ndc |
| ndc11 | package | 58264005401 | derived:openfda.package_ndc |
| spl id | 2b9ec8dd-73ab-e366-e063-6394a90ae792 | id | |
| spl set id | 68a206a8-6f66-4957-843c-4c4c0636e78f | set_id | |
| unii | 27YLU75U4W | openfda.unii | |
| unii | CI71S98N1Z | openfda.unii | |
| unii | QDL83WN8C2 | openfda.unii | |
| unii | 639KR60Q1Q | openfda.unii | |
| unii | S7V92P67HO | openfda.unii | |
| unii | WQZ3G9PF0H | openfda.unii | |
| unii | Y0F0BU8RDU | openfda.unii | |
| unii | C88X29Y479 | 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.