NDC 50017-032-01 - 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: 50017-032
Requested NDC: 50017-032-01
Package NDCs from labels: 50017-032-01, 50017-032-02
Manufacturer: Neat Feat Products Limited
Effective date: 2025-01-08
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Willow Wart - Neat Feat Products Limited	Neat Feat Products Limited	2025-01-08	HUMAN OTC DRUG LABEL

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
50017-032	WILLOW WART (SALIX ALBA, THUJA OCCIDENTALIS) CREAM [NEAT FEAT PRODUCTS LIMITED]	6	Legacy NDC	20250110_897dcd1a-8fea-7bbf-e053-2995a90a185e.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 168 of 168 · 3,342 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
CVS Hand Sanitizer	ALCOHOL	CVS	d0081c50-c0d2-436a-ba83-5d1982ae64b7	2015-08-17	Warnings	Exact identifier unii: 3K9958V90M
Instant Hand Sanitizer	ALCOHOL	Safetec of America, Inc.	f9e30645-491b-4f54-acfd-f863ee235607	2013-08-07	Warnings	Exact identifier unii: 3K9958V90M

Reported adverse events (FAERS/openFDA)#

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