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  5. NDC Package Code: 55714-2419-1 Detoxifier

NDC Package 55714-2419-1 Detoxifier

Uricum Acidum,Benzoicum Acidum,Berber. Vulg.,Bryonia,Cantharis,Carduus - 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:
55714-2419-1
Package Description:
28 g in 1 BOTTLE, GLASS
Product Code:
55714-2419
Proprietary Name:
Detoxifier
Non-Proprietary Name:
Uricum Acidum, Benzoicum Acidum, Berber. Vulg., Bryonia, Cantharis, Carduus Benedictus, Ceanothus, Chelidonium Majus, Chionanthus Virginica, Cinchona, Dioscorea, Dolichos, Iris Versicolor, Juniperus Com., Nux Vom., Ptelea, Taraxacum, Carduus Mar., Cynara Scolymus, Solidago
Substance Name:
Benzoic Acid; Berberis Vulgaris Root Bark; Bryonia Alba Root; Ceanothus Americanus Leaf; Centaurea Benedicta; Chelidonium Majus; Chionanthus Virginicus Bark; Cinchona Officinalis Bark; Cynara Scolymus Leaf; Dioscorea Villosa Tuber; Iris Versicolor Root; Juniper Berry; Lytta Vesicatoria; Mucuna Pruriens Fruit Trichome; Ptelea Trifoliata Bark; Silybum Marianum Seed; Solidago Virgaurea Flowering Top; Strychnos Nux-vomica Seed; Taraxacum Officinale; Uric Acid
Usage Information:
Formulated for symptoms associated with toxicity such as fatigue, headaches and sluggish elimination.
11-Digit NDC Billing Format:
55714241901
Product Type:
Human Otc Drug
Labeler Name:
Newton Laboratories, Inc.
Dosage Form:
Pellet - A small sterile solid mass consisting of a highly purified drug (with or without excipients) made by the formation of granules, or by compression and molding.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • BENZOIC ACID 10 [hp_X]/g
  • BERBERIS VULGARIS ROOT BARK 10 [hp_X]/g
  • BRYONIA ALBA ROOT 10 [hp_X]/g
  • CEANOTHUS AMERICANUS LEAF 10 [hp_X]/g
  • CENTAUREA BENEDICTA 10 [hp_X]/g
  • CHELIDONIUM MAJUS 10 [hp_X]/g
  • CHIONANTHUS VIRGINICUS BARK 10 [hp_X]/g
  • CINCHONA OFFICINALIS BARK 10 [hp_X]/g
  • CYNARA SCOLYMUS LEAF 6 [hp_X]/g
  • DIOSCOREA VILLOSA TUBER 10 [hp_X]/g
  • IRIS VERSICOLOR ROOT 10 [hp_X]/g
  • JUNIPER BERRY 10 [hp_X]/g
  • LYTTA VESICATORIA 10 [hp_X]/g
  • MUCUNA PRURIENS FRUIT TRICHOME 10 [hp_X]/g
  • PTELEA TRIFOLIATA BARK 10 [hp_X]/g
  • SILYBUM MARIANUM SEED 10 [hp_X]/g
  • SOLIDAGO VIRGAUREA FLOWERING TOP 6 [hp_X]/g
  • STRYCHNOS NUX-VOMICA SEED 15 [hp_X]/g
  • TARAXACUM OFFICINALE 10 [hp_X]/g
  • URIC ACID 15 [hp_X]/g
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Allergens - [CS]
  • Ammonium Ion Binding Activity - [MoA] (Mechanism of Action)
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Dietary Proteins - [CS]
  • Food Additives - [CS]
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Increased IgG Production - [PE] (Physiologic Effect)
  • Nitrogen Binding Agent - [EPC] (Established Pharmacologic Class)
  • Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Plant Proteins - [CS]
  • Seed Storage Proteins - [CS]
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    01-31-2019
    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 55714-2419-1?

    The NDC Packaged Code 55714-2419-1 is assigned to a package of 28 g in 1 bottle, glass of Detoxifier, a human over the counter drug labeled by Newton Laboratories, Inc.. The product's dosage form is pellet and is administered via oral form.

    Is NDC 55714-2419 included in the NDC Directory?

    Yes, Detoxifier with product code 55714-2419 is active and included in the NDC Directory. The product was first marketed by Newton Laboratories, Inc. on January 31, 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 55714-2419-1?

    The 11-digit format is 55714241901. 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
    5-4-155714-2419-15-4-255714-2419-01