NDC11 43857061301

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
43857-0613-01	43857-0613
43857-0613-1	43857-0613
43857-613-01	43857-613

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
Bio Chem Detox	BERBERIS VULGARIS, GLYCYRRHIZA GLABRA, LAPPA MAJOR, RHAMNUS PURSHIANA, STILLINGIA SYLVATICA, TRIFOLIUM PRATENSE, TRITICUM AESTIVUM, XANTHOXYLUM FRAXINEUM, PHYTOLACCA DECANDRA, GLANDULA SUPRARENALIS SUIS, HEPAR SUIS, LYMPH NODE (SUIS), THYROIDINUM (SUIS), LYCOPODIUM CLAVATUM, NUX VOMICA, PHOSPHORICUM ACIDUM, ACONITUM NAPELLUS, ARSENICUM ALBUM, BELLADONNA, CARBO VEGETABILIS, CINCHONA OFFICINALIS, CONIUM MACULATUM, MERCURIUS CORROSIVUS, PHOSPHORUS, SULPHUR, TABACUM, NITRICUM ACIDUM, AGARICUS MUSCARIUS,	BioActive Nutritional, Inc.	3f9bd6c8-6fc9-4af1-8263-ab42f99fba37	2026-03-05	Warnings	Exact identifier ndc (package): 43857-0613-1 ndc (product): 43857-0613 ndc11 (package): 43857061301

Reported adverse events (FAERS/openFDA)#

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