NDC11 13411085660

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
13411-0856-60	13411-0856
13411-856-60	13411-856

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
JBA Joint Revive	GLUCOSAMINE SULFATE POTASSIUM CHLORIDE,WHITE WILLOW BARK EXTRACT,EGGSHELL MEMBRANE COLLAGEN,CHONDROITIN SULFATE,TURMERIC ROOT EXTRACT,BROMELAIN,SOY LECITHIN	Advanced Pharmaceutical Services, Inc. Dba Affordable Quality Pharmaceuticals	27f5acf3-04f6-49d7-bbf5-f1c3ad6200cc	2025-03-31	Warnings	Exact identifier ndc (package): 13411-856-60 ndc (product): 13411-856 ndc11 (package): 13411085660

Reported adverse events (FAERS/openFDA)#

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