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  5. NDC Package Code: 55758-318-02 Desintox

NDC Package 55758-318-02 Desintox

Antimonium Crudum, Argentum Nitricum, Cholesterinum,Robinia Pseudo-acacia, Carbo - 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:
55758-318-02
Package Description:
1 BOTTLE in 1 BOX / 60 mL in 1 BOTTLE
Product Code:
55758-318
Proprietary Name:
Desintox
Non-Proprietary Name:
Antimonium Crudum, Argentum Nitricum, Cholesterinum, Robinia Pseudo-acacia, Carbo Vegetabilis, Cinchona, Aesculus Hippocastanum, Arnica Montana, Berberis Vulgaris, Ceanothus Americanus, Cynara Scolymus, Equisetum Arvense, Erigeron Canadensis, Fucus Vesiculosus, Ginkgo Biloba, Hamamelis Virginiana, Helonias Dioica, Hydrastis Canadensis, Hydrastis Canadensis, Lappa Major, Lespedeza Capitata, Raphanus Sativus, Taraxacum Officinale, Viburnum Prunifolium, Vitis Vinifera, Ranunculus Bulbosus
Substance Name:
Activated Charcoal; Antimony Trisulfide; Arctium Lappa Root; Arnica Montana; Berberis Vulgaris Root Bark; Ceanothus Americanus Leaf; Chamaelirium Luteum Root; Cinchona Bark; Cynara Scolymus Leaf; Equisetum Arvense Top; Erigeron Canadensis; Fucus Vesiculosus; Ginkgo; Goldenseal; Hamamelis Virginiana Root Bark/stem Bark; Horse Chestnut; Lespedeza Capitata Flowering Top; Radish; Ranunculus Bulbosus; Robinia Pseudoacacia Bark; Silver Nitrate; Taraxacum Officinale; Viburnum Prunifolium Bark; Vitis Vinifera Whole
Usage Information:
Shake well before each useadults and children over 12 years of age: place 20 drops in a small glass of water two (2) times a day, 15 minutes before a mealallow medicine to remain in the mouth for 15 seconds before swallowing
11-Digit NDC Billing Format:
55758031802
Product Type:
Human Otc Drug
Labeler Name:
Pharmadel Llc
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.
    • Active Ingredient(s):
  • ACTIVATED CHARCOAL 9 [hp_X]/60mL
  • ANTIMONY TRISULFIDE 10 [hp_X]/60mL
  • ARCTIUM LAPPA ROOT 6 [hp_X]/60mL
  • ARNICA MONTANA 6 [hp_X]/60mL
  • BERBERIS VULGARIS ROOT BARK 6 [hp_X]/60mL
  • CEANOTHUS AMERICANUS LEAF 6 [hp_X]/60mL
  • CHAMAELIRIUM LUTEUM ROOT 6 [hp_X]/60mL
  • CINCHONA BARK 8 [hp_X]/60mL
  • CYNARA SCOLYMUS LEAF 6 [hp_X]/60mL
  • EQUISETUM ARVENSE TOP 6 [hp_X]/60mL
  • ERIGERON CANADENSIS 6 [hp_X]/60mL
  • FUCUS VESICULOSUS 6 [hp_X]/60mL
  • GINKGO 10 [hp_X]/60mL
  • GOLDENSEAL 6 [hp_X]/60mL
  • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 6 [hp_X]/60mL
  • HORSE CHESTNUT 6 [hp_X]/60mL
  • LESPEDEZA CAPITATA FLOWERING TOP 6 [hp_X]/60mL
  • RADISH 6 [hp_X]/60mL
  • RANUNCULUS BULBOSUS 4 [hp_X]/60mL
  • ROBINIA PSEUDOACACIA BARK 10 [hp_X]/60mL
  • SILVER NITRATE 10 [hp_X]/60mL
  • TARAXACUM OFFICINALE 6 [hp_X]/60mL
  • VIBURNUM PRUNIFOLIUM BARK 6 [hp_X]/60mL
  • VITIS VINIFERA WHOLE 6 [hp_X]/60mL
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Dietary Proteins - [CS]
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Vegetable Proteins - [CS]
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    01-01-2019
    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 55758-318-02?

    The NDC Packaged Code 55758-318-02 is assigned to a package of 1 bottle in 1 box / 60 ml in 1 bottle of Desintox, a human over the counter drug labeled by Pharmadel Llc. The product's dosage form is liquid and is administered via oral form.

    Is NDC 55758-318 included in the NDC Directory?

    Yes, Desintox with product code 55758-318 is active and included in the NDC Directory. The product was first marketed by Pharmadel Llc on January 01, 2019 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 11-digit format for NDC 55758-318-02?

    The 11-digit format is 55758031802. 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 5-3-2 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
    5-3-255758-318-025-4-255758-0318-02