Home FDA labels 807a024f-1eb0-48f1-aed9-dcbde843d8c3 Diathesis V 2 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 V 2
Generic name GINKGO BILOBA, PANCREAS SUIS, SPLEEN (SUIS), STOMACH (SUIS), GERMANIUM SESQUIOXIDE, COBALTUM METALLICUM, CYSTEINUM, NICCOLUM METALLICUM, ZINCUM METALLICUM, MANGANESE GLUCONATE, ALPHA-KETOGLUTARICUM ACIDUM, BARYTA CARBONICA, FUMARICUM ACIDUM, NATRUM OXALACETICUM, PHOSPHORICUM ACIDUM, PHOSPHORUS
Manufacturer BioActive Nutritional, Inc.
Product type HUMAN OTC DRUG
SPL set ID 1f389621-b22b-4d6c-9c28-93292eb4eebf
SPL ID 807a024f-1eb0-48f1-aed9-dcbde843d8c3
Version 1
Effective date 2024-02-13
Source export date 2026-11-06
Source partition 8
Source file https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-11-06/9d5577a314a25811fefbde4767c9b37f3913d9a65fdc458c6336b5aed532339e/drug-label-0008-of-0014.json.zip
Source manifest SHA-256 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run 20261106T075659Z
Imported at 2026-11-06 08:52:20 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 · 24 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Diathesis V 2 openfda.brand_name generic name GINKGO BILOBA, PANCREAS SUIS, SPLEEN (SUIS), STOMACH (SUIS), GERMANIUM SESQUIOXIDE, COBALTUM METALLICUM, CYSTEINUM, NICCOLUM METALLICUM, ZINCUM METALLICUM, MANGANESE GLUCONATE, ALPHA-KETOGLUTARICUM ACIDUM, BARYTA CARBONICA, FUMARICUM ACIDUM, NATRUM OXALACETICUM, PHOSPHORICUM ACIDUM, PHOSPHORUS openfda.generic_name manufacturer name BioActive Nutritional, Inc. openfda.manufacturer_name ndc package 43857-0638-1 openfda.package_ndc ndc product 43857-0638 openfda.product_ndc ndc11 package 43857063801 derived:openfda.package_ndc spl id 807a024f-1eb0-48f1-aed9-dcbde843d8c3 id spl set id 1f389621-b22b-4d6c-9c28-93292eb4eebf set_id unii 27YLU75U4W openfda.unii unii T0920P9Z9A openfda.unii unii 8ID597Z82X openfda.unii unii 9YY2F980SV openfda.unii unii 96WE91N25T openfda.unii unii 88XHZ13131 openfda.unii unii 6P669D8HQ8 openfda.unii unii 3G0H8C9362 openfda.unii unii K848JZ4886 openfda.unii unii 92AMN5J79Y openfda.unii unii 7OV03QG267 openfda.unii unii 19FUJ2C58T openfda.unii unii E4GA8884NN openfda.unii unii 6CA025Y4FG openfda.unii unii J41CSQ7QDS openfda.unii unii 9Y3J3362RY 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.