NDC11 85948025102

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
85948-0251-02	85948-0251
85948-0251-2	85948-0251
85948-251-02	85948-251

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
LEBELAGE UV SUN ULTRA SHIELD SUN SCREENLOTION 50g	AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTOCRYLENE, OCTISALATE	DONGDONGGURIMOO CO.,LTD.	4907eb9c-3978-27ed-e063-6394a90a9f66	2026-01-22	Warnings	Exact identifier ndc (package): 85948-251-02 ndc (product): 85948-251 ndc11 (package): 85948025102

Reported adverse events (FAERS/openFDA)#

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