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-107
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-107
- Generic name
- ACTAEA SPICATA ROOT, ARNICA MONTANA, CAULOPHYLLUM THALICTROIDES ROOT, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, OXALIC ACID, SEPIA OFFICINALIS JUICE, COLA ACUMINATA SEED, STELLARIA MEDIA, AND TOXICODENDRON PUBESCENS LEAF
- Manufacturer
- DNA Labs, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- e12a693d-cf0b-48d6-9317-a54d146005e0
- SPL ID
- 2b9ed994-a888-0e65-e063-6394a90aca84
- Version
- 3
- Effective date
- 2025-01-13
- Source export date
- 2026-10-12
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:02:12
| 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-107 | openfda.brand_name | |
| generic name | ACTAEA SPICATA ROOT, ARNICA MONTANA, CAULOPHYLLUM THALICTROIDES ROOT, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, OXALIC ACID, SEPIA OFFICINALIS JUICE, COLA ACUMINATA SEED, STELLARIA MEDIA, AND TOXICODENDRON PUBESCENS LEAF | openfda.generic_name | |
| manufacturer name | DNA Labs, Inc. | openfda.manufacturer_name | |
| ndc | package | 58264-0113-1 | openfda.package_ndc |
| ndc | product | 58264-0113 | openfda.product_ndc |
| ndc11 | package | 58264011301 | derived:openfda.package_ndc |
| spl id | 2b9ed994-a888-0e65-e063-6394a90aca84 | id | |
| spl set id | e12a693d-cf0b-48d6-9317-a54d146005e0 | set_id | |
| unii | 1F8VIW1479 | openfda.unii | |
| unii | O80TY208ZW | openfda.unii | |
| unii | 2H03479QVR | openfda.unii | |
| unii | JTJ6HH6YEH | openfda.unii | |
| unii | QDL83WN8C2 | openfda.unii | |
| unii | HF539G9L3Q | openfda.unii | |
| unii | 9E7R5L6H31 | openfda.unii | |
| unii | 6IO182RP7A | openfda.unii | |
| unii | 3FU86L9OS0 | 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.