NDC11 82157001501

This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.

Possible FDA NDC forms#

Package NDC, Product root table
Package NDC	Product root
82157-0015-01	82157-0015
82157-0015-1	82157-0015
82157-015-01	82157-015

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 1 of 1 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
nioxin PRO CLINICAL SCALP RECOVERY scalp soothing serum	PYRITHIONE ZINC	The Wella Corporation	31ce9b5c-d388-8e1d-e063-6294a90a2fb8	2025-11-25	Warnings	Exact identifier ndc (package): 82157-015-01 ndc (product): 82157-015 ndc11 (package): 82157001501
nioxin PRO CLINICAL SCALP RECOVERY	PYRITHIONE ZINC	Wella Operations US LLC	31bf4f7f-8228-7433-e063-6394a90a2f5f	2025-11-25	Warnings	Exact identifier ndc (package): 82157-015-01 ndc11 (package): 82157001501

Reported adverse events (FAERS/openFDA)#

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