NDC11 69777024001

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
69777-0240-01	69777-0240
69777-0240-1	69777-0240
69777-240-01	69777-240

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
OrgaPlus Ultra Pure Sun EX 15g	OCTINOXATE, OCTISALATE, OCTOCRYLENE	BLUEZONWIDE CO.,LTD	b686ef63-7eee-4a4d-a559-417d8b09cc4f	2025-02-05	Warnings	Exact identifier ndc (package): 69777-240-01 ndc (product): 69777-240 ndc11 (package): 69777024001

Reported adverse events (FAERS/openFDA)#

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