NDC11 43742197001

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
43742-1970-01	43742-1970
43742-1970-1	43742-1970

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
Detox III	DULCAMARA, ECHINACEA (ANGUSTIFOLIA), AESCULUS HIPPOCASTANUM, ANTIMONIUM TARTARICUM, ASCORBICUM ACIDUM, COCCUS CACTI, GALIUM APARINE, GENTIANA LUTEA, GERANIUM ROBERTIANUM, PULSATILLA (PRATENSIS), SARCOLACTICUM ACIDUM, CONIUM MACULATUM, LYMPH NODE (SUIS), SULPHUR, GLANDULA SUPRARENALIS SUIS, L-PHENYLALANINE, CALCAREA PHOSPHORICA, FERRUM PHOSPHORICUM, HEPAR SUIS, HYPOTHALAMUS SUIS, SPLEEN (SUIS), CORTISONE ACETICUM, MERCURIUS SOLUBILIS, BARYTA CARBONICA, GLYPHOSATE, FUNICULUS UMBILICALIS SUIS,TONSIL (SUIS),	Deseret Biologicals, Inc.	6f2136ce-4763-4ebd-a9fc-cbbae1f7ce0b	2024-02-19	Warnings	Exact identifier ndc (package): 43742-1970-1 ndc (product): 43742-1970 ndc11 (package): 43742197001

Reported adverse events (FAERS/openFDA)#

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