warnings
Warnings If pregnant or breast-feeding, consult a health professional before use. In case of accidental overdose, seek professional assistance or contact a poison control center immediately.
Rubus
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
- Rubus
- Generic name
- RUBUS FRUTICOSUS, IRIS GERMANICA, VACCINIUM MYRTILLUS, SYZYGIUM JAMBOLANUM, OKOUBAKA AUBREVILLEI
- Manufacturer
- Marco Pharma International LLC.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- bcaf8cd2-3880-4dd7-9895-d33e63c1a229
- SPL ID
- 483b8e1e-a66f-9470-e063-6294a90af6a3
- Version
- 5
- Effective date
- 2026-01-12
- 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 02:02:13
| Harmonized routes |
|---|
| ORAL |
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 | Rubus | openfda.brand_name | |
| generic name | RUBUS FRUTICOSUS, IRIS GERMANICA, VACCINIUM MYRTILLUS, SYZYGIUM JAMBOLANUM, OKOUBAKA AUBREVILLEI | openfda.generic_name | |
| manufacturer name | Marco Pharma International LLC. | openfda.manufacturer_name | |
| ndc | package | 60986-1011-3 | openfda.package_ndc |
| ndc | package | 60986-1011-4 | openfda.package_ndc |
| ndc | product | 60986-1011 | openfda.product_ndc |
| ndc11 | package | 60986101103 | derived:openfda.package_ndc |
| ndc11 | package | 60986101104 | derived:openfda.package_ndc |
| spl id | 483b8e1e-a66f-9470-e063-6294a90af6a3 | id | |
| spl set id | bcaf8cd2-3880-4dd7-9895-d33e63c1a229 | set_id | |
| unii | 820LSF646I | openfda.unii | |
| unii | 8A6OMU3I8L | openfda.unii | |
| unii | MK2074187Z | openfda.unii | |
| unii | 9P2U39H18W | openfda.unii | |
| unii | 8N6VTJ9IWV | 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.