Diathesis
- Product NDC
- 43857-0148
- 11-digit product format
- 438570148
- Labeler code
- 43857
- Product ID
- 43857-0148_bd91c732-4a58-4ec2-872c-7164485e30c3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Heart (Suis), Small Intestine (Suis), Germanium Sesquioxide, Cobaltum Metallicum, Cysteinum, Manganum Metallicum, Manganese Gluconate, alpha-Ketoglutaricum Acidum, Arsenicum Album, Aurum Metallicum, Fumaricum Acidum, Natrum Oxalaceticum, Phosphorus
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- BioActive Nutritional, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2013-04-16
- Substance
- .ALPHA.-KETOGLUTARIC ACID; ARSENIC TRIOXIDE; COBALT; CYSTEINE; FUMARIC ACID; GERMANIUM SESQUIOXIDE; GOLD; MANGANESE; MANGANESE GLUCONATE; PHOSPHORUS; PORK HEART; PORK INTESTINE; SODIUM DIETHYL OXALACETATE
- Active strength
- 12; 12; 9; 9; 12; 8; 12; 9; 10; 12; 6; 6; 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
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Diathesis
- Brand name suffix
- III
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| PORK HEART | 12 [hp_X]/mL |
| PORK INTESTINE | 12 [hp_X]/mL |
| GERMANIUM SESQUIOXIDE | 9 [hp_X]/mL |
| COBALT | 9 [hp_X]/mL |
| CYSTEINE | 12 [hp_X]/mL |
| MANGANESE | 8 [hp_X]/mL |
| MANGANESE GLUCONATE | 12 [hp_X]/mL |
| .ALPHA.-KETOGLUTARIC ACID | 9 [hp_X]/mL |
| ARSENIC TRIOXIDE | 10 [hp_X]/mL |
| GOLD | 12 [hp_X]/mL |
| FUMARIC ACID | 6 [hp_X]/mL |
| SODIUM DIETHYL OXALACETATE | 6 [hp_X]/mL |
| PHOSPHORUS | 12 [hp_X]/mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| X876KJM95L | Internal UNII lookup |
| 40GMI0R60L | Internal UNII lookup |
| 96WE91N25T | Internal UNII lookup |
| 3G0H8C9362 | Internal UNII lookup |
| K848JZ4886 | Internal UNII lookup |
| 42Z2K6ZL8P | Internal UNII lookup |
| 9YY2F980SV | Internal UNII lookup |
| 8ID597Z82X | Internal UNII lookup |
| S7V92P67HO | Internal UNII lookup |
| 79Y1949PYO | Internal UNII lookup |
| 88XHZ13131 | Internal UNII lookup |
| 6CA025Y4FG | Internal UNII lookup |
| 27YLU75U4W | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| d914f6d6-5008-4153-81d3-87a297ac5d20 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 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 |
|---|---|---|---|---|---|---|
| 43857-0148-1 | DiathesisIII | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 43857-0148 | DIATHESIS III (HEART (SUIS), SMALL INTESTINE (SUIS), GERMANIUM SESQUIOXIDE, COBALTUM METALLICUM, CYSTEINUM, MANGANUM METALLICUM, MANGANESE GLUCONATE, ALPHA-KETOGLUTARICUM ACIDUM, ARSENICUM ALBUM, AURUM METALLICUM, FUMARICUM ACIDUM, NATRUM OXALACETICUM, PHOSPHORUS) LIQUID [BIOACTIVE NUTRITIONAL, INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20171018_d914f6d6-5008-4153-81d3-87a297ac5d20.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 III | HEART (SUIS), SMALL INTESTINE (SUIS), GERMANIUM SESQUIOXIDE, COBALTUM METALLICUM, CYSTEINUM, MANGANUM METALLICUM, MANGANESE GLUCONATE, ALPHA-KETOGLUTARICUM ACIDUM, ARSENICUM ALBUM, AURUM METALLICUM, FUMARICUM ACIDUM, NATRUM OXALACETICUM, PHOSPHORUS | BioActive Nutritional, Inc. | d914f6d6-5008-4153-81d3-87a297ac5d20 | 2026-04-27 | Warnings | 43857-0148 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 43857-0148-1 | 43857014801 | 30 mL in 1 BOTTLE, DROPPER (43857-0148-1) | 30 ml | 2013-04-16 | 0000-00-00 | No | No | Current |