NDC11 87556000301

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 NDCProduct root
87556-0003-0187556-0003
87556-0003-187556-0003
87556-003-0187556-003

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 ยท 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SPESOLSKII WART CORN CALLUS REMOVERSALICYLIC ACID 17% WART CORN CALLUS REMOVERBEST GREEN LIMITED588463b3-9314-226f-e063-6394a90a012d2026-08-08WarningsExact identifier
ndc (package): 87556-003-01
ndc (product): 87556-003
ndc11 (package): 87556000301

Reported adverse events (FAERS/openFDA)#

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