NDC11 87534015001

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
87534-0150-01	87534-0150
87534-0150-1	87534-0150
87534-150-01	87534-150

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 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ULTRA SOOTHER DRY-TOUCH SUNSCREEN	HOMOSALATE, OCTISALATE, OCTOCRYLENE, ZINC OXIDE	skinnplus	4dbc1035-c41c-308c-e063-6394a90a36c4	2026-03-23	Warnings	Exact identifier ndc (package): 87534-150-01 ndc (product): 87534-150 ndc11 (package): 87534015001

Reported adverse events (FAERS/openFDA)#

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