Diathesis
- Product NDC
- 43857-0372
- 11-digit product format
- 438570372
- Labeler code
- 43857
- Product ID
- 43857-0372_e9e9be76-4b66-42b5-80de-bea58b041b1b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Germanium Sesquioxide, Cuprum Metallicum, Manganum Metallicum, Intestine (Suis), Lung (Suis), Cysteinum, Manganese Gluconate, alpha-Ketoglutaricum Acidum, Arsenicum Album, Calcarea Carbonica, Fumaricum Acidum, Natrum Oxalaceticum, Phosphorus
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- BioActive Nutritional, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-07-09
- Substance
- GERMANIUM SESQUIOXIDE; COPPER; MANGANESE; PORK INTESTINE; SUS SCROFA LUNG; CYSTEINE; MANGANESE GLUCONATE; OXOGLURIC ACID; ARSENIC TRIOXIDE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; FUMARIC ACID; SODIUM DIETHYL OXALACETATE; PHOSPHORUS
- Active strength
- 8; 8; 8; 8; 8; 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
- Pharmacologic classes
- Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Inhibit Ovum Fertilization [PE], Magnetic Resonance Contrast Activity [MoA], Paramagnetic Contrast Agent [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
- Brand name suffix
- II
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| GERMANIUM SESQUIOXIDE | 8 [hp_X]/mL |
| COPPER | 8 [hp_X]/mL |
| MANGANESE | 8 [hp_X]/mL |
| PORK INTESTINE | 8 [hp_X]/mL |
| SUS SCROFA LUNG | 8 [hp_X]/mL |
| CYSTEINE | 9 [hp_X]/mL |
| MANGANESE GLUCONATE | 10 [hp_X]/mL |
| OXOGLURIC ACID | 12 [hp_X]/mL |
| ARSENIC TRIOXIDE | 12 [hp_X]/mL |
| OYSTER SHELL CALCIUM CARBONATE, CRUDE | 12 [hp_X]/mL |
| FUMARIC ACID | 12 [hp_X]/mL |
| SODIUM DIETHYL OXALACETATE | 12 [hp_X]/mL |
| PHOSPHORUS | 12 [hp_X]/mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 96WE91N25T | Internal UNII lookup |
| 789U1901C5 | Internal UNII lookup |
| 42Z2K6ZL8P | Internal UNII lookup |
| 40GMI0R60L | Internal UNII lookup |
| 7GL3G1COB3 | Internal UNII lookup |
| K848JZ4886 | Internal UNII lookup |
| 9YY2F980SV | Internal UNII lookup |
| 8ID597Z82X | Internal UNII lookup |
| S7V92P67HO | Internal UNII lookup |
| 2E32821G6I | Internal UNII lookup |
| 88XHZ13131 | Internal UNII lookup |
| 6CA025Y4FG | Internal UNII lookup |
| 27YLU75U4W | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 240a5573-0603-4201-ab11-39b894b8794e | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| c599c4a0-705d-4ebb-ab1f-977af038f96a | Product name | 1 | 20251124 |
| 63f39a63-5cd1-4016-bd86-2bbb0f6c3139 | Product name | 3 | 20240506 |
| e5a77e9c-c528-733a-173d-914a234c024b | Product name | 5 | 20240506 |
| 503ea967-4b9c-48cf-9e87-c7975295849d | Product name | 2 | 20220120 |
| 2e254488-9fcb-41b3-a7c3-e2c9a3941b29 | Product name | 1 | 20200603 |
| b4ff0805-126a-406d-9cae-fc34fd8e8889 | Product name | 1 | 20190711 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 43857-0372-1 | DiathesisII | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 43857-0372 | DIATHESIS II (GERMANIUM SESQUIOXIDE, CUPRUM METALLICUM, MANGANUM METALLICUM, INTESTINE (SUIS), LUNG (SUIS), CYSTEINUM, MANGANESE GLUCONATE, ALPHA-KETOGLUTARICUM ACIDUM, ARSENICUM ALBUM, CALCAREA CARBONICA, FUMARICUM ACIDUM, NATRUM OXALACETICUM, PHOSPHORUS) LIQUID [BIOACTIVE NUTRITIONAL, INC.] | 2 | Current NDC, Legacy NDC, 1 package rows | 20171228_240a5573-0603-4201-ab11-39b894b8794e.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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Diathesis II | GERMANIUM SESQUIOXIDE, CUPRUM METALLICUM, MANGANUM METALLICUM, INTESTINE (SUIS), LUNG (SUIS), CYSTEINUM, MANGANESE GLUCONATE, ALPHA-KETOGLUTARICUM ACIDUM, ARSENICUM ALBUM, CALCAREA CARBONICA, FUMARICUM ACIDUM, NATRUM OXALACETICUM, PHOSPHORUS | BioActive Nutritional, Inc. | 240a5573-0603-4201-ab11-39b894b8794e | 2017-12-27 | Warnings | 43857-0372 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 43857-0372-1 | 43857037201 | 30 mL in 1 BOTTLE, DROPPER (43857-0372-1) | 30 ml | 2015-07-09 | 0000-00-00 | No | No | Current |