Kidney Tonic Liquid
NDC Package 43857-0579-1
Package Information
Kidney Tonic (glutathione, kidney (suis), urinary bladder (suis), agrimonia eupatoria flos, apis mellifica, berberis vulgaris, bryonia (alba), calcarea carbonica, galium aparine, rubia tinctorum) liquids is for temporary relief of burning pain in the region of the kidneys, sticking pain in the region of the kidneys, radiatingaround the abdomen and groin, frequent urination with painin the thighs and loins. This formulation utilizes a liquid delivery system. Marketed by Bioactive Nutritional, Inc., this product is identified by NDC 43857-0579.
Identification & Billing
Clinical Specifications
- AGRIMONIA EUPATORIA FLOWER 8 [hp_X]/mL
- APIS MELLIFERA 12 [hp_X]/mL
- BERBERIS VULGARIS ROOT BARK 12 [hp_X]/mL
- BRYONIA ALBA WHOLE 12 [hp_X]/mL
- GALIUM APARINE WHOLE 12 [hp_X]/mL
- GLUTATHIONE 6 [hp_X]/mL
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/mL
- PORK KIDNEY 6 [hp_X]/mL
- RUBIA TINCTORUM ROOT 12 [hp_X]/mL
- SUS SCROFA URINARY BLADDER 6 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 43857 - Bioactive Nutritional, Inc.
- 43857-0579 - Kidney Tonic
- 43857-0579-1 - 60 mL in 1 BOTTLE, DROPPER
- 43857-0579 - Kidney Tonic
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 43857-0579-1 identifies a specific commercial package of 60 ml in 1 bottle, dropper of Kidney Tonic II, a human over the counter drug labeled by Bioactive Nutritional, Inc.. This liquid is formulated for oral use and contains agrimonia eupatoria flower; apis mellifera; berberis vulgaris root bark; bryonia alba whole; galium aparine whole; glutathione; oyster shell calcium carbonate, crude; pork kidney; rubia tinctorum root; sus scrofa urinary bladder 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 Nutritional, Inc. on February 18, 2021. The current certification is valid through December 31, 2027.
How is this Bioactive Nutritional, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 43857057901. 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.