Bladder Kidney Meridian Opener Liquid
NDC Package 43742-0836-1
Package Information
Bladder Kidney Meridian Opener (apis mellifica, argentum nitricum, berberis vulgaris, cantharis, equisetum arvense, kali bichromicum, lycopodium clavatum, mercurius solubilis, natrum muriaticum, phosphorus, rhus tox, sepia, terebinthina, thuja occidentalis) liquids is for temporary relief of symptoms related to irregular menses, and pain or burning.****These statements are based upon traditional homeopathic practice. This formulation utilizes a liquid delivery system. Marketed by Deseret Biologicals, Inc., this product is identified by NDC 43742-0836.
Identification & Billing
Clinical Specifications
- APIS MELLIFERA 30 [hp_C]/mL
- BERBERIS VULGARIS ROOT BARK 30 [hp_C]/mL
- EQUISETUM ARVENSE TOP 30 [hp_C]/mL
- LYCOPODIUM CLAVATUM SPORE 30 [hp_C]/mL
- LYTTA VESICATORIA 30 [hp_C]/mL
- MERCURIUS SOLUBILIS 30 [hp_C]/mL
- PHOSPHORUS 30 [hp_C]/mL
- POTASSIUM DICHROMATE 30 [hp_C]/mL
- SEPIA OFFICINALIS JUICE 30 [hp_C]/mL
- SILVER NITRATE 30 [hp_C]/mL
- SODIUM CHLORIDE 30 [hp_C]/mL
- THUJA OCCIDENTALIS LEAF 30 [hp_C]/mL
- TOXICODENDRON PUBESCENS LEAF 30 [hp_C]/mL
- TURPENTINE OIL 30 [hp_C]/mL
Regulatory & Marketing
Hierarchy Structure
- 43742 - Deseret Biologicals, Inc.
- 43742-0836 - Bladder Kidney Meridian Opener
- 43742-0836-1 - 30 mL in 1 BOTTLE, DROPPER
- 43742-0836 - Bladder Kidney Meridian Opener
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 43742-0836-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Bladder Kidney Meridian Opener, a human over the counter drug labeled by Deseret Biologicals, Inc.. This liquid is formulated for oral use and contains apis mellifera; berberis vulgaris root bark; equisetum arvense top; lycopodium clavatum spore; lytta vesicatoria; mercurius solubilis; phosphorus; potassium dichromate; sepia officinalis juice; silver nitrate; sodium chloride; thuja occidentalis leaf; toxicodendron pubescens leaf; turpentine oil 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 Deseret Biologicals, Inc. on August 19, 2016. The current certification is valid through December 31, 2026.
How is this Deseret Biologicals, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 43742083601. 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.