NDC11 72220000203

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
72220-0002-03	72220-0002
72220-0002-3	72220-0002
72220-002-03	72220-002

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
MDP PEPTIDE 9 BIO SUN PRO	HOMOSALATE, OCTOCRYLENE, ETHYLHEXYL SALICYLATE, BUTYL METHOXYDIBENZOYLMETHANE	SKINIDEA CO., LTD	26db53cd-dd82-8790-e063-6394a90a92b1	2026-07-03	Warnings	Exact identifier ndc (package): 72220-002-03 ndc (product): 72220-002 ndc11 (package): 72220000203

Reported adverse events (FAERS/openFDA)#

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