FDA.reportPublic FDA data

Diathesis

Product NDC
43857-0631
11-digit product format
438570631
Labeler code
43857
Product ID
43857-0631_610e5fa0-b73b-4643-9f99-bd65d59f8b3f
Type
HUMAN OTC DRUG
Nonproprietary 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
Dosage form
LIQUID
Route
ORAL
Labeler
BioActive Nutritional, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-04-13
Substance
BOS TAURUS BILE; COPPER; CYSTEINE; FUMARIC ACID; GERMANIUM SESQUIOXIDE; GINKGO; GOLD; MANGANESE GLUCONATE; MERCURIUS SOLUBILIS; OXOGLURIC ACID; PHOSPHORIC ACID; PORK KIDNEY; SILVER; SODIUM DIETHYL OXALACETATE; STRYCHNOS NUX-VOMICA SEED
Active strength
6; 9; 9; 12; 8; 6; 9; 10; 12; 12; 12; 6; 9; 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
Pharmacologic classes
Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Inhibit Ovum Fertilization [PE], Magnetic Resonance Contrast Activity [MoA], Non-Standardized Plant Allergenic Extract [EPC], Paramagnetic Contrast Agent [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Standardized Chemical Allergen [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Diathesis
Brand name suffix
IV
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
GINKGO6 [hp_X]/mL
BOS TAURUS BILE9 [hp_X]/mL
PORK KIDNEY9 [hp_X]/mL
GERMANIUM SESQUIOXIDE12 [hp_X]/mL
SILVER8 [hp_X]/mL
COPPER6 [hp_X]/mL
CYSTEINE9 [hp_X]/mL
GOLD10 [hp_X]/mL
MANGANESE GLUCONATE12 [hp_X]/mL
OXOGLURIC ACID12 [hp_X]/mL
FUMARIC ACID12 [hp_X]/mL
MERCURIUS SOLUBILIS6 [hp_X]/mL
SODIUM DIETHYL OXALACETATE9 [hp_X]/mL
STRYCHNOS NUX-VOMICA SEED12 [hp_X]/mL
PHOSPHORIC ACID12 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 15 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
19FUJ2C58TInternal UNII lookup
ET3651ZLOUInternal UNII lookup
X7BCI5P86HInternal UNII lookup
96WE91N25TInternal UNII lookup
3M4G523W1GInternal UNII lookup
789U1901C5Internal UNII lookup
K848JZ4886Internal UNII lookup
79Y1949PYOInternal UNII lookup
9YY2F980SVInternal UNII lookup
8ID597Z82XInternal UNII lookup
88XHZ13131Internal UNII lookup
324Y4038G2Internal UNII lookup
6CA025Y4FGInternal UNII lookup
269XH13919Internal UNII lookup
E4GA8884NNInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
74b5157f-c33f-494a-ab61-0e0a547b5f4aAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c599c4a0-705d-4ebb-ab1f-977af038f96aProduct name120251124
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
43857-0631-1DiathesisIV30 mL in 1 BOTTLE, DROPPERLIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43857-0631DIATHESIS IV (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) LIQUID [BIOACTIVE NUTRITIONAL, INC.]1Current NDC, 1 package rows20230414_74b5157f-c33f-494a-ab61-0e0a547b5f4a.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 IVGINKGO 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 ACIDUMBioActive Nutritional, Inc.74b5157f-c33f-494a-ab61-0e0a547b5f4a2023-04-13WarningsExact identifier
ndc (product): 43857-0631

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
43857-0631-14385706310130 mL in 1 BOTTLE, DROPPER (43857-0631-1) 30 ml2023-04-13NoNoCurrent