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. To be used according to standard homeopathic indications.
T-22
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
- T-22
- Generic name
- QUERCUS ROBUR WHOLE
- Manufacturer
- DNA Labs, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 652e3c71-0fe2-420e-8c75-90a2ff88d87c
- SPL ID
- 2b539e1c-6629-f6dc-e063-6294a90a587d
- Version
- 5
- Effective date
- 2025-01-09
- Source export date
- 2026-10-12
- Source partition
- 1
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/7928c8e8c6256620071a8b7e5b93eb8dfa543649c08d17a01ea02251012ba58c/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:25:17
| 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 | T-22 | openfda.brand_name | |
| generic name | QUERCUS ROBUR WHOLE | openfda.generic_name | |
| manufacturer name | DNA Labs, Inc. | openfda.manufacturer_name | |
| ndc | package | 58264-0267-1 | openfda.package_ndc |
| ndc | product | 58264-0267 | openfda.product_ndc |
| ndc11 | package | 58264026701 | derived:openfda.package_ndc |
| spl id | 2b539e1c-6629-f6dc-e063-6294a90a587d | id | |
| spl set id | 652e3c71-0fe2-420e-8c75-90a2ff88d87c | set_id | |
| unii | R7QMG0BT2W | 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.