warnings
Warnings For external use only.
REINREUDE MULTI-PURPOSE TREATMENT
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
- REINREUDE MULTI-PURPOSE TREATMENT
- Generic name
- TOLNAFTATE 1% MULTI-PURPOSE TREATMENT
- Manufacturer
- Jiangxi Yudexi Pharmaceutical Co., LTD
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 4a380945-9235-783a-e063-6294a90a094d
- SPL ID
- 57295f18-04f7-adc0-e063-6394a90ae048
- Version
- 2
- Effective date
- 2026-07-21
- Source export date
- 2026-09-28
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:15:25
| Harmonized routes |
|---|
| TOPICAL |
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 |
|---|---|---|---|
| application number | M005 | openfda.application_number | |
| brand name | REINREUDE MULTI-PURPOSE TREATMENT | openfda.brand_name | |
| generic name | TOLNAFTATE 1% MULTI-PURPOSE TREATMENT | openfda.generic_name | |
| manufacturer name | Jiangxi Yudexi Pharmaceutical Co., LTD | openfda.manufacturer_name | |
| ndc | package | 85248-072-01 | openfda.package_ndc |
| ndc | product | 85248-072 | openfda.product_ndc |
| ndc11 | package | 85248007201 | derived:openfda.package_ndc |
| rxcui | 313423 | openfda.rxcui | |
| spl id | 57295f18-04f7-adc0-e063-6394a90ae048 | id | |
| spl set id | 4a380945-9235-783a-e063-6294a90a094d | set_id | |
| unii | 06KB629TKV | 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.