FDA.reportPublic FDA data

NDC 82309-032-01 - Willow Wart

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
82309-032
Requested NDC
82309-032-01
Package NDCs from labels
82309-032-01, 82309-032-02
Manufacturer
Tripak Pharmaceuticals
Effective date
2023-12-18
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Willow Wart - Tripak PharmaceuticalsTripak Pharmaceuticals2023-12-18HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82309-032-022025-01-30C16284748780-1f386c64a-3396-0266-e053-dadaa90a7c1aWillow Wart
82309-032-022023-12-18C16284748780-1f386c64a-3396-0266-e053-dadaa90a7c1aWillow Wart
82309-032-022023-01-30C16284748780-1f386c64a-3396-0266-e053-dadaa90a7c1aWillow Wart

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82309-032-01Willow Wart10 g in 1 TUBECREAM105
82309-032-02Willow Wart1 in 1 BOXCREAM15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82309-032WILLOW WART (SALIX ALBA, THUJA OCCIDENTALIS) CREAM [TRIPAK PHARMACEUTICALS]5Legacy NDC, 2 package rows20231219_d2185a5a-fc6f-c816-e053-2995a90ae496.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 166 of 166 · 3,304 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Eye WashWATERCVS Pharmacy049cee29-7ec2-4d5b-8308-f522acde43a72017-03-29WarningsExact identifier
unii: 059QF0KO0R
Sterile WaterWATERBaxter Healthcare Company210dc9ab-d6ca-4552-ac19-1be17792d2902016-05-31Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
CVS Hand SanitizerALCOHOLCVSd0081c50-c0d2-436a-ba83-5d1982ae64b72015-08-17WarningsExact identifier
unii: 3K9958V90M
Instant Hand SanitizerALCOHOLSafetec of America, Inc.f9e30645-491b-4f54-acfd-f863ee2356072013-08-07WarningsExact identifier
unii: 3K9958V90M

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.