NDC11 60232003501

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
60232-0035-01	60232-0035
60232-0035-1	60232-0035
60232-035-01	60232-035

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
Private Label SPF 50 80 min Water Resistant	HOMOSALATE, OCTISALATE, ZINC OXIDE SUNSCREEN	Swiss-American CDMO, LLC	8849fa88-24c8-410d-b16e-60da38288f98	2023-11-14	Warnings	Exact identifier ndc (package): 60232-0035-1 ndc (product): 60232-0035 ndc11 (package): 60232003501

Reported adverse events (FAERS/openFDA)#

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