NDC11 84938001401

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
84938-0014-01	84938-0014
84938-0014-1	84938-0014
84938-014-01	84938-014

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
SUNSCREEN SPRAY150mL	ZINC OXIDE 12%, TITANIUM DIOXIDE 6%, HOMOSALATE 14%, OCTISALATE 5%	Foshan Sugar Max Cosmetics CO.,Ltd	4635f90a-bbc9-0676-e063-6394a90a9f35	2025-12-18	Warnings	Exact identifier ndc (package): 84938-014-01 ndc (product): 84938-014 ndc11 (package): 84938001401

Reported adverse events (FAERS/openFDA)#

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