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.
T-7
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-7
- Generic name
- AESCULUS HIPPOCASTANUM WHOLE
- Manufacturer
- DNA Labs, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 90f63c08-05af-495b-b109-f905cdd52b53
- SPL ID
- 2b539b74-75a9-e36c-e063-6294a90ae2dd
- Version
- 5
- Effective date
- 2025-01-09
- Source export date
- 2026-09-28
- Source partition
- 13
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:36:55
| 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-7 | openfda.brand_name | |
| generic name | AESCULUS HIPPOCASTANUM WHOLE | openfda.generic_name | |
| manufacturer name | DNA Labs, Inc. | openfda.manufacturer_name | |
| ndc | package | 58264-0252-1 | openfda.package_ndc |
| ndc | product | 58264-0252 | openfda.product_ndc |
| ndc11 | package | 58264025201 | derived:openfda.package_ndc |
| spl id | 2b539b74-75a9-e36c-e063-6294a90ae2dd | id | |
| spl set id | 90f63c08-05af-495b-b109-f905cdd52b53 | set_id | |
| unii | 2331W47PSX | 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.