NDC11 49757001022

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
49757-0010-22	49757-0010
49757-010-22	49757-010

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
Sunscreen SPF 50	AVOBENZONE 3% , HOMOSALATE 10%,OCTISALATE 5%	Rocky Mountain	9647b817-653f-45e5-b71a-ee9ad82e84eb	2026-03-18	Warnings	Exact identifier ndc (package): 49757-010-22 ndc (product): 49757-010 ndc11 (package): 49757001022

Reported adverse events (FAERS/openFDA)#

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