NDC11 69683020211

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
69683-0202-11	69683-0202
69683-202-11	69683-202

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
DERMOSCRIBE SEBORRHEIC DERMATITIS	SULFUR, SALICYLIC ACID, HYDROCORTISONE	DERMOSCRIBE PTY LTD	2b6bf90b-5d42-4c08-afee-56e13122285e	2025-10-17	Warnings	Exact identifier ndc (package): 69683-202-11 ndc (product): 69683-202 ndc11 (package): 69683020211

Reported adverse events (FAERS/openFDA)#

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