NDC Package 43742-1582-1 Bio Lymph Phase

Scrophularia Nodosa,Teucrium Scorodonia,Veronica Officinalis,Equisetum Hyemale,Fumaria - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
43742-1582-1
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
Proprietary Name:
Bio Lymph Phase
Non-Proprietary Name:
Scrophularia Nodosa, Teucrium Scorodonia, Veronica Officinalis, Equisetum Hyemale, Fumaria Officinalis, Geranium Robertianum, Nasturtium Aquaticum, Natrum Sulphuricum, Pinus Sylvestris, Gentiana Lutea, Juglans Regia, Aranea Diadema, Sarsaparilla (smilax Regelii), Ascorbicum Acidum, Quercetin, Myosotis Arvensis, Calcarea Phosphorica, Ferrum Iodatum, Thyroidinum (suis), Gaertner Bacillus (bach)
Substance Name:
Araneus Diadematus; Ascorbic Acid; Equisetum Hyemale; Ferrous Iodide; Fumaria Officinalis Flowering Top; Gentiana Lutea Root; Geranium Robertianum; Juglans Regia Leaf; Myosotis Arvensis; Nasturtium Officinale; Pinus Sylvestris Leafy Twig; Quercetin; Salmonella Enterica Enterica Serovar Enteritidis; Scrophularia Nodosa; Smilax Ornata Root; Sodium Sulfate; Teucrium Scorodonia Flowering Top; Thyroid, Porcine; Tribasic Calcium Phosphate; Veronica Officinalis Flowering Top
Usage Information:
For the temporary relief of swelling due to minor injury.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration. For the temporary relief of swelling due to minor injury.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
11-Digit NDC Billing Format:
43742158201
Product Type:
Human Otc Drug
Labeler Name:
Deseret Biologicals, Inc.
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(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    01-14-2020
    End Marketing Date:
    01-02-2025
    Exclude Flag:
    N
    Code Structure:

    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 disclaimer below.

    Frequently Asked Questions

    What is NDC 43742-1582-1?

    The NDC Packaged Code 43742-1582-1 is assigned to a package of 30 ml in 1 bottle, dropper of Bio Lymph Phase, a human over the counter drug labeled by Deseret Biologicals, Inc.. The product's dosage form is liquid and is administered via oral form.

    Is NDC 43742-1582 included in the NDC Directory?

    Yes, Bio Lymph Phase with product code 43742-1582 is active and included in the NDC Directory. The product was first marketed by Deseret Biologicals, Inc. on January 14, 2020.

    What is the 11-digit format for NDC 43742-1582-1?

    The 11-digit format is 43742158201. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-4-143742-1582-15-4-243742-1582-01