FDA.reportPublic FDA data

Diathesis V 2

Product NDC
43857-0638
11-digit product format
438570638
Labeler code
43857
Product ID
43857-0638_807a024f-1eb0-48f1-aed9-dcbde843d8c3
Type
HUMAN OTC DRUG
Nonproprietary 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
Dosage form
LIQUID
Route
ORAL
Labeler
BioActive Nutritional, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2024-02-13
Substance
GINKGO; SUS SCROFA PANCREAS; SUS SCROFA SPLEEN; SUS SCROFA STOMACH; GERMANIUM SESQUIOXIDE; COBALT; CYSTEINE; NICKEL; ZINC; MANGANESE GLUCONATE, UNSPECIFIED FORM; OXOGLURIC ACID; BARIUM CARBONATE; FUMARIC ACID; SODIUM DIETHYL OXALACETATE; PHOSPHORIC ACID; PHOSPHORUS
Active strength
6; 6; 6; 6; 8; 9; 9; 9; 9; 10; 12; 12; 12; 12; 12; 12 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes
Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Magnetic Resonance Contrast Activity [MoA], Paramagnetic Contrast Agent [EPC], Standardized Chemical Allergen [EPC], Standardized Chemical Allergen [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
Diathesis V 2
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
GINKGO6 [hp_X]/mL
SUS SCROFA PANCREAS6 [hp_X]/mL
SUS SCROFA SPLEEN6 [hp_X]/mL
SUS SCROFA STOMACH6 [hp_X]/mL
GERMANIUM SESQUIOXIDE8 [hp_X]/mL
COBALT9 [hp_X]/mL
CYSTEINE9 [hp_X]/mL
NICKEL9 [hp_X]/mL
ZINC9 [hp_X]/mL
MANGANESE GLUCONATE, UNSPECIFIED FORM10 [hp_X]/mL
OXOGLURIC ACID12 [hp_X]/mL
BARIUM CARBONATE12 [hp_X]/mL
FUMARIC ACID12 [hp_X]/mL
SODIUM DIETHYL OXALACETATE12 [hp_X]/mL
PHOSPHORIC ACID12 [hp_X]/mL
PHOSPHORUS12 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 16 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
19FUJ2C58TInternal UNII lookup
9Y3J3362RYInternal UNII lookup
92AMN5J79YInternal UNII lookup
T0920P9Z9AInternal UNII lookup
96WE91N25TInternal UNII lookup
3G0H8C9362Internal UNII lookup
K848JZ4886Internal UNII lookup
7OV03QG267Internal UNII lookup
J41CSQ7QDSInternal UNII lookup
9YY2F980SVInternal UNII lookup
8ID597Z82XInternal UNII lookup
6P669D8HQ8Internal UNII lookup
88XHZ13131Internal UNII lookup
6CA025Y4FGInternal UNII lookup
E4GA8884NNInternal UNII lookup
27YLU75U4WInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1f389621-b22b-4d6c-9c28-93292eb4eebfAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
2e254488-9fcb-41b3-a7c3-e2c9a3941b29Product name120200603
b4ff0805-126a-406d-9cae-fc34fd8e8889Product name120190711

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43857-0638-1Diathesis V 230 mL in 1 BOTTLE, DROPPERLIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43857-0638DIATHESIS V 2 (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) LIQUID [BIOACTIVE NUTRITIONAL, INC.]1Current NDC, 1 package rows20240328_1f389621-b22b-4d6c-9c28-93292eb4eebf.zip

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Diathesis V 2GINKGO 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, PHOSPHORUSBioActive Nutritional, Inc.1f389621-b22b-4d6c-9c28-93292eb4eebf2024-02-13WarningsExact identifier
ndc (product): 43857-0638

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
43857-0638-14385706380130 mL in 1 BOTTLE, DROPPER (43857-0638-1) 30 ml2024-02-13NoNoCurrent