Diathesis Liquid
NDC Package 43857-0249-1
Package Information
Diathesis (manganum metallicum, germanium sesquioxide, fel tauri, hepar suis, ginkgo biloba, cysteinum, manganese gluconate, alpha-ketoglutaricum acidum, arsenicum album, fumaricum acidum, phosphorus, sodium oxalate, sulphur) liquids is for temporary relief of inflammation of bones or joints, with nightly digging pains, general soreness and aching soreness over entire body when touched, and burning in soles and hands at night. This formulation utilizes a liquid delivery system. Marketed by Bioactive Nutritionals, Inc., this product is identified by NDC 43857-0249.
Identification & Billing
Clinical Specifications
- .ALPHA.-KETOGLUTARIC ACID 12 [hp_X]/mL
- ARSENIC TRIOXIDE 12 [hp_X]/mL
- BOS TAURUS BILE 6 [hp_X]/mL
- CYSTEINE 9 [hp_X]/mL
- FUMARIC ACID 12 [hp_X]/mL
- GERMANIUM SESQUIOXIDE 8 [hp_X]/mL
- GINKGO 6 [hp_X]/mL
- MANGANESE 9 [hp_X]/mL
- MANGANESE GLUCONATE 10 [hp_X]/mL
- PHOSPHORUS 12 [hp_X]/mL
- PORK LIVER 6 [hp_X]/mL
- SODIUM OXALATE 12 [hp_X]/mL
- SULFUR 12 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 43857 - Bioactive Nutritionals, Inc.
- 43857-0249 - Diathesis
- 43857-0249-1 - 30 mL in 1 BOTTLE, DROPPER
- 43857-0249 - Diathesis
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 43857-0249-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Diathesis I, a human over the counter drug labeled by Bioactive Nutritionals, Inc.. This liquid is formulated for oral use and contains .alpha.-ketoglutaric acid; arsenic trioxide; bos taurus bile; cysteine; fumaric acid; germanium sesquioxide; ginkgo; manganese; manganese gluconate; phosphorus; pork liver; sodium oxalate; sulfur as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Bioactive Nutritionals, Inc. on January 09, 2014. The current certification is valid through December 31, 2026.
How is this Bioactive Nutritionals, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 43857024901. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.