NDC11 62795101003

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
62795-1010-03	62795-1010
62795-1010-3	62795-1010

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
BHI Arthritis	ARNICA MONTANA ROOT, BERBERIS VULGARIS ROOT BARK, BRYONIA ALBA WHOLE, CAUSTICUM, CITRULLUS COLOCYNTHIS FRUIT PULP, SOLANUM DULCAMARA TOP, FERROSOFERRIC PHOSPHATE, LEDUM PALUSTRE TWIG, LYCOPODIUM CLAVATUM SPORE, RANUNCULUS BULBOSUS, RHODODENDRON AUREUM LEAF, TOXICODENDRON PUBESCENS LEAF , AND SULFUR	MediNatura Inc	d58c4651-2871-4beb-b1f5-e01a793cbc44	2024-12-17	Warnings	Exact identifier ndc (package): 62795-1010-3 ndc (product): 62795-1010 ndc11 (package): 62795101003

Reported adverse events (FAERS/openFDA)#

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