NDC11 75936062102

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
75936-0621-02	75936-0621
75936-0621-2	75936-0621
75936-621-02	75936-621

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
Triple Prep SPF 40	AVOBENZONE, OCTISALATE, OCTOCRYLENE, HOMOSALATE	Supergoop, LLC	004df4e5-dba9-6030-e063-6394a90a76d3	2026-01-09	Warnings	Exact identifier ndc (package): 75936-621-02 ndc (product): 75936-621 ndc11 (package): 75936062102

Reported adverse events (FAERS/openFDA)#

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