Lymph Liquid
NDC Package 43857-0552-1

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Lymph (echinacea (angustifolia), collinsonia canadensis, phytolacca decandra, kali iodatum, pinus sylvestris, pix liquida, ferrum phosphoricum, aesculus hippocastanum, baryta carbonica, berberis vulgaris, calcarea carbonica, calcarea phosphorica, causticum, hepar sulphuris calcareum, kreosotum, lycopodium clavatum, mercurius solubilis, natrum muriaticum, nitricum acidum, phosphorus, pulsatilla (pratensis), silicea, stellaria media, sulphur, terebinthina, thuja occidentalis, bufo rana) liquids is for temporary relief of glandular swelling with inflammation and induration, glands hot, swollen, painful; scrofulous swelling, axillary glands swollen with soreness of the upper arm and tonsils. This formulation utilizes a liquid delivery system. Marketed by Bioactive Nutritional, Inc., this product is identified by NDC 43857-0552.

Identification & Billing

NDC Package Code
43857-0552-1
Package Description
60 mL in 1 BOTTLE, DROPPER
Product Code
43857-0552
11-Digit Billing Format
43857055201

Clinical Specifications

Proprietary Name
Lymph II
Non-Proprietary Name
Echinacea (angustifolia), Collinsonia Canadensis, Phytolacca Decandra, Kali Iodatum, Pinus Sylvestris, Pix Liquida, Ferrum Phosphoricum, Aesculus Hippocastanum, Baryta Carbonica, Berberis Vulgaris, Calcarea Carbonica, Calcarea Phosphorica, Causticum, Hepar Sulphuris Calcareum, Kreosotum, Lycopodium Clavatum, Mercurius Solubilis, Natrum Muriaticum, Nitricum Acidum, Phosphorus, Pulsatilla (pratensis), Silicea, Stellaria Media, Sulphur, Terebinthina, Thuja Occidentalis, Bufo Rana
Substance Name
Echinacea Angustifolia Whole; Collinsonia Canadensis Root; Phytolacca Americana Root; Potassium Iodide; Pinus Sylvestris Leafy Twig; Pine Tar; Ferrosoferric Phosphate; Horse Chestnut; Barium Carbonate; Berberis Vulgaris Root Bark; Oyster Shell Calcium Carbonate, Crude; Tribasic Calcium Phosphate; Causticum; Calcium Sulfide; Wood Creosote; Lycopodium Clavatum Spore; Mercurius Solubilis; Sodium Chloride; Nitric Acid; Phosphorus; Pulsatilla Pratensis Whole; Silicon Dioxide; Stellaria Media; Sulfur; Turpentine Oil; Thuja Occidentalis Leafy Twig; Bufo Bufo Cutaneous Gland
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
For temporary relief of glandular swelling with inflammation and induration, glands hot, swollen, painful; scrofulous swelling, axillary glands swollen with soreness of the upper arm and tonsils. For temporary relief of glandular swelling with inflammation and induration, glands hot, swollen, painful; scrofulous swelling, axillary glands swollen with soreness of the upper arm and tonsils.

Regulatory & Marketing

Labeler Name
Bioactive Nutritional, Inc.
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
03-18-2020
End Marketing Date
09-05-2029
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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.

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 43857-0552-1 identifies a specific commercial package of 60 ml in 1 bottle, dropper of Lymph II, a human over the counter drug labeled by Bioactive Nutritional, Inc.. This liquid is formulated for oral use and contains echinacea angustifolia whole; collinsonia canadensis root; phytolacca americana root; potassium iodide; pinus sylvestris leafy twig; pine tar; ferrosoferric phosphate; horse chestnut; barium carbonate; berberis vulgaris root bark; oyster shell calcium carbonate, crude; tribasic calcium phosphate; causticum; calcium sulfide; wood creosote; lycopodium clavatum spore; mercurius solubilis; sodium chloride; nitric acid; phosphorus; pulsatilla pratensis whole; silicon dioxide; stellaria media; sulfur; turpentine oil; thuja occidentalis leafy twig; bufo bufo cutaneous gland 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 March 18, 2020.

How is this Bioactive Nutritional, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 43857055201. 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:

10-Digit Format (5-4-1)
43857-0552-1
11-Digit CMS (5-4-2)
43857-0552-01

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.