Home FDA labels 610e5fa0-b73b-4643-9f99-bd65d59f8b3f Diathesis IV openFDA label record# This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)
Brand name Diathesis IV
Generic name GINKGO BILOBA, FEL TAURI, KIDNEY (SUIS), GERMANIUM SESQUIOXIDE, ARGENTUM METALLICUM, CUPRUM METALLICUM, CYSTEINUM, AURUM METALLICUM, MANGANESE GLUCONATE, ALPHA-KETOGLUTARICUM ACIDUM, FUMARICUM ACIDUM, MERCURIUS SOLUBILIS, NATRUM OXALACETICUM, NUX VOMICA, PHOSPHORICUM ACIDUM
Manufacturer BioActive Nutritional, Inc.
Product type HUMAN OTC DRUG
SPL set ID 74b5157f-c33f-494a-ab61-0e0a547b5f4a
SPL ID 610e5fa0-b73b-4643-9f99-bd65d59f8b3f
Version 1
Effective date 2023-04-13
Source export date 2026-09-28
Source partition 14
Source file https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:41:03 Harmonized routes table Harmonized routes ORAL
Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 23 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Diathesis IV openfda.brand_name generic name GINKGO BILOBA, FEL TAURI, KIDNEY (SUIS), GERMANIUM SESQUIOXIDE, ARGENTUM METALLICUM, CUPRUM METALLICUM, CYSTEINUM, AURUM METALLICUM, MANGANESE GLUCONATE, ALPHA-KETOGLUTARICUM ACIDUM, FUMARICUM ACIDUM, MERCURIUS SOLUBILIS, NATRUM OXALACETICUM, NUX VOMICA, PHOSPHORICUM ACIDUM openfda.generic_name manufacturer name BioActive Nutritional, Inc. openfda.manufacturer_name ndc package 43857-0631-1 openfda.package_ndc ndc product 43857-0631 openfda.product_ndc ndc11 package 43857063101 derived:openfda.package_ndc spl id 610e5fa0-b73b-4643-9f99-bd65d59f8b3f id spl set id 74b5157f-c33f-494a-ab61-0e0a547b5f4a set_id unii 8ID597Z82X openfda.unii unii 9YY2F980SV openfda.unii unii 3M4G523W1G openfda.unii unii 789U1901C5 openfda.unii unii 269XH13919 openfda.unii unii 96WE91N25T openfda.unii unii 88XHZ13131 openfda.unii unii ET3651ZLOU openfda.unii unii 324Y4038G2 openfda.unii unii 79Y1949PYO openfda.unii unii X7BCI5P86H openfda.unii unii K848JZ4886 openfda.unii unii 19FUJ2C58T openfda.unii unii E4GA8884NN openfda.unii unii 6CA025Y4FG openfda.unii
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings sections page 1 of 1 · 1 matching rows.
warnings WARNINGS: If pregnant or breast-feeding, ask a health care professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is broken or missing. Store in cool, dry place.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.