NDC11 49967089504

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
49967-0895-04	49967-0895
49967-0895-4	49967-0895
49967-895-04	49967-895

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
Kiehls Since 1851 Dermatologist Solutions Breakout Control Targeted Acne Spot Treatment	SULFUR	L'Oreal USA Products Inc	217c697e-0260-46d5-a202-ce7345eadd94	2023-12-30	Warnings	Exact identifier ndc (package): 49967-895-04 ndc (product): 49967-895 ndc11 (package): 49967089504

Reported adverse events (FAERS/openFDA)#

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