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  5. NDC Package Code: 62795-9491-2 Lymphomyosot

NDC Package 62795-9491-2 Lymphomyosot

Araneus Diadematus,Tribasic Calcium Phosphate, Equisetum Hyemale Whole,Ferrous Iodide, - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
62795-9491-2
Package Description:
1 BOTTLE in 1 CARTON / 100 TABLET in 1 BOTTLE
Product Code:
62795-9491
Proprietary Name:
Lymphomyosot
Non-Proprietary Name:
Araneus Diadematus, Tribasic Calcium Phosphate, Equisetum Hyemale Whole, Ferrous Iodide, Fumaria Officinalis Flowering Top, Gentiana Lutea Root, Juglans Regia Leaf, Levothyroxine Sodium Anhydrous, Myosotis Arvensis Whole, Nasturtium Officinale, Sodium Sulfate, Pinus Sylvestris Leafy Twig, Smilax Ornata Root, Scrophularia Nodosa Whole, Teucrium Scorodonia Flowering, Veronica Officinalis Flowering Top
Substance Name:
Araneus Diadematus; Equisetum Hyemale Whole; Ferrous Iodide; Fumaria Officinalis Flowering Top; Gentiana Lutea Root; Geranium Robertianum; Juglans Regia Leaf; Levothyroxine Sodium Anhydrous; Myosotis Arvensis Whole; Nasturtium Officinale; Pinus Sylvestris Leafy Twig; Scrophularia Nodosa Whole; Smilax Ornata Root; Sodium Sulfate; Teucrium Scorodonia Flowering Top; Tribasic Calcium Phosphate; Veronica Officinalis Flowering Top
Usage Information:
Adults and children 4 years andolder: 1-2 tablets 3 times per day or as directed by ahealth practitioner. Not to exceed 6 tablets per 24hours. Children under 4, as directed by a healthprofessional. Allow to completely dissolve in the mouth.
11-Digit NDC Billing Format:
62795949102
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
1 EA
Product Type:
Human Otc Drug
Labeler Name:
Medinatura Inc
Dosage Form:
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ARANEUS DIADEMATUS 6 [hp_X]/1
  • EQUISETUM HYEMALE WHOLE 4 [hp_X]/1
  • FERROUS IODIDE 12 [hp_X]/1
  • FUMARIA OFFICINALIS FLOWERING TOP 4 [hp_X]/1
  • GENTIANA LUTEA ROOT 5 [hp_X]/1
  • GERANIUM ROBERTIANUM 4 [hp_X]/1
  • JUGLANS REGIA LEAF 3 [hp_X]/1
  • LEVOTHYROXINE SODIUM ANHYDROUS 12 [hp_X]/1
  • MYOSOTIS ARVENSIS WHOLE 3 [hp_X]/1
  • NASTURTIUM OFFICINALE 4 [hp_X]/1
  • PINUS SYLVESTRIS LEAFY TWIG 4 [hp_X]/1
  • SCROPHULARIA NODOSA WHOLE 3 [hp_X]/1
  • SMILAX ORNATA ROOT 6 [hp_X]/1
  • SODIUM SULFATE 4 [hp_X]/1
  • TEUCRIUM SCORODONIA FLOWERING TOP 3 [hp_X]/1
  • TRIBASIC CALCIUM PHOSPHATE 12 [hp_X]/1
  • VERONICA OFFICINALIS FLOWERING TOP 3 [hp_X]/1
    • Pharmacologic Class(es):
  • Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
  • Calcium - [CS]
  • Cations, Divalent - [CS]
  • Increased Coagulation Factor Activity - [PE] (Physiologic Effect)
  • Phosphate Binder - [EPC] (Established Pharmacologic Class)
  • Phosphate Chelating Activity - [MoA] (Mechanism of Action)
  • Thyroxine - [CS]
  • l-Thyroxine - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    02-16-2022
    Listing Expiration Date:
    12-31-2024
    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 62795-9491-2?

    The NDC Packaged Code 62795-9491-2 is assigned to a package of 1 bottle in 1 carton / 100 tablet in 1 bottle of Lymphomyosot, a human over the counter drug labeled by Medinatura Inc. The product's dosage form is tablet and is administered via oral form.This product is billed for "EA" each discreet unit and contains an estimated amount of 1 billable units per package.

    Is NDC 62795-9491 included in the NDC Directory?

    Yes, Lymphomyosot with product code 62795-9491 is active and included in the NDC Directory. The product was first marketed by Medinatura Inc on February 16, 2022 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 62795-9491-2?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 1.

    What is the 11-digit format for NDC 62795-9491-2?

    The 11-digit format is 62795949102. 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
    5-4-162795-9491-25-4-262795-9491-02