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-105
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-105
- Generic name
- BOS TAURUS ADRENAL GLAND, APIS MELLIFERA, ARSENIC TRIOXIDE, LYTTA VESICATORIA, BOS TAURUS LYMPH VESSEL, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, TOXICODENDRON PUBESCENS LEAF, URTICA URENS, PYRIDOXINE HYDROCHLORIDE, AND ASCORBIC ACID
- Manufacturer
- DNA Labs, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 1535cb47-b155-4ac4-af7d-b22ac8325403
- SPL ID
- 2b9ef9ce-f828-5195-e063-6294a90a28c2
- Version
- 3
- Effective date
- 2025-01-13
- Source export date
- 2026-10-12
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:29:10
| 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-105 | openfda.brand_name | |
| generic name | BOS TAURUS ADRENAL GLAND, APIS MELLIFERA, ARSENIC TRIOXIDE, LYTTA VESICATORIA, BOS TAURUS LYMPH VESSEL, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, TOXICODENDRON PUBESCENS LEAF, URTICA URENS, PYRIDOXINE HYDROCHLORIDE, AND ASCORBIC ACID | openfda.generic_name | |
| manufacturer name | DNA Labs, Inc. | openfda.manufacturer_name | |
| ndc | package | 58264-0111-1 | openfda.package_ndc |
| ndc | product | 58264-0111 | openfda.product_ndc |
| ndc11 | package | 58264011101 | derived:openfda.package_ndc |
| spl id | 2b9ef9ce-f828-5195-e063-6294a90a28c2 | id | |
| spl set id | 1535cb47-b155-4ac4-af7d-b22ac8325403 | set_id | |
| unii | HF539G9L3Q | openfda.unii | |
| unii | 3Q034RO3BT | openfda.unii | |
| unii | IHN2NQ5OF9 | openfda.unii | |
| unii | PQ6CK8PD0R | openfda.unii | |
| unii | 6IO182RP7A | openfda.unii | |
| unii | S7V92P67HO | openfda.unii | |
| unii | 85I1Z426OV | openfda.unii | |
| unii | M2776SWB29 | openfda.unii | |
| unii | 7S82P3R43Z | openfda.unii | |
| unii | 68Y4CF58BV | 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.