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-110
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-110
- Generic name
- ARNICA MONTANA, HYPERICUM PERFORATUM, PHOSPHORUS, RANCID BEEF, RUTA GRAVEOLENS FLOWERING TOP, FERROSOFERRIC PHOSPHATE, LACHESIS MUTA VENOM, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, AND CALENDULA OFFICINALIS FLOWERING TOP
- Manufacturer
- DNA Labs, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 780ec514-9e36-4a4c-b947-960888fa7c75
- SPL ID
- 2b9ef26a-132c-fdee-e063-6394a90abb13
- Version
- 3
- Effective date
- 2025-01-13
- Source export date
- 2026-09-28
- 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/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:07:34
| 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-110 | openfda.brand_name | |
| generic name | ARNICA MONTANA, HYPERICUM PERFORATUM, PHOSPHORUS, RANCID BEEF, RUTA GRAVEOLENS FLOWERING TOP, FERROSOFERRIC PHOSPHATE, LACHESIS MUTA VENOM, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, AND CALENDULA OFFICINALIS FLOWERING TOP | openfda.generic_name | |
| manufacturer name | DNA Labs, Inc. | openfda.manufacturer_name | |
| ndc | package | 58264-0116-1 | openfda.package_ndc |
| ndc | product | 58264-0116 | openfda.product_ndc |
| ndc11 | package | 58264011601 | derived:openfda.package_ndc |
| spl id | 2b9ef26a-132c-fdee-e063-6394a90abb13 | id | |
| spl set id | 780ec514-9e36-4a4c-b947-960888fa7c75 | set_id | |
| unii | 27YLU75U4W | openfda.unii | |
| unii | XK4IUX8MNB | openfda.unii | |
| unii | O80TY208ZW | openfda.unii | |
| unii | 18E7415PXQ | openfda.unii | |
| unii | N94C2U587S | openfda.unii | |
| unii | 29SUH5R3HU | openfda.unii | |
| unii | 91GQH8I5F7 | openfda.unii | |
| unii | VSW71SS07I | openfda.unii | |
| unii | T7S323PKJS | 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.