NDC11 49527008402

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
49527-0084-02	49527-0084
49527-0084-2	49527-0084
49527-084-02	49527-084

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
MOISTURE SURGE SPF	AVOBENZONE,HOMOSALATE,OCTINOXATE,OCTISALATE	CLINIQUE LABORATORIES LLC	ec921e21-db68-db77-e053-2a95a90a5781	2025-08-15	Warnings	Exact identifier ndc (package): 49527-084-02 ndc (product): 49527-084 ndc11 (package): 49527008402

Reported adverse events (FAERS/openFDA)#

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