Lymphastat B Liquid
NDC Package 44911-0682-1
Package Information
Lymphastat B (baptisia tinctoria, echinacea (angustifolia), phytolacca decandra, aconitum napellus, arsenicum album, belladonna, ferrum phosphoricum, lachesis mutus, mercurius corrosivus, phosphorus, colibacillinum cum natrum muriaticum, pyrogenium) liquids is adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. This formulation utilizes a liquid delivery system. Marketed by Energique, Inc., this product is identified by NDC 44911-0682.
Identification & Billing
Clinical Specifications
- ACONITUM NAPELLUS WHOLE 12 [hp_X]/mL
- ARSENIC TRIOXIDE 12 [hp_X]/mL
- ATROPA BELLADONNA 12 [hp_X]/mL
- BAPTISIA TINCTORIA ROOT 3 [hp_X]/mL
- ECHINACEA ANGUSTIFOLIA WHOLE 3 [hp_X]/mL
- ESCHERICHIA COLI 30 [hp_X]/mL
- FERROSOFERRIC PHOSPHATE 12 [hp_X]/mL
- LACHESIS MUTA VENOM 12 [hp_X]/mL
- MERCURIC CHLORIDE 12 [hp_X]/mL
- PHOSPHORUS 12 [hp_X]/mL
- PHYTOLACCA AMERICANA ROOT 6 [hp_X]/mL
- RANCID BEEF 30 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 44911 - Energique, Inc.
- 44911-0682 - Lymphastat B
- 44911-0682-1 - 60 mL in 1 BOTTLE, DROPPER
- 44911-0682 - Lymphastat B
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 44911-0682-1 identifies a specific commercial package of 60 ml in 1 bottle, dropper of Lymphastat B, a human over the counter drug labeled by Energique, Inc.. This liquid is formulated for oral use and contains aconitum napellus whole; arsenic trioxide; atropa belladonna; baptisia tinctoria root; echinacea angustifolia whole; escherichia coli; ferrosoferric phosphate; lachesis muta venom; mercuric chloride; phosphorus; phytolacca americana root; rancid beef 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 Energique, Inc. on October 10, 2023. The current certification is valid through December 31, 2026.
How is this Energique, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 44911068201. 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.