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  5. NDC Package Code: 58264-0140-1 D134

NDC Package 58264-0140-1 D134

Black Cohosh,Bryonia Alba Whole,Toxicodendron Pubescens Whole,Arnica - 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:
58264-0140-1
Package Description:
29.57 mL in 1 BOTTLE, GLASS
Product Code:
58264-0140
Proprietary Name:
D134
Non-Proprietary Name:
Black Cohosh, Bryonia Alba Whole, Toxicodendron Pubescens Whole, Arnica Montana, Causticum, Ferrosoferric Phosphate, Sodium Sulfate Anhydrous, Strychnos Nux-vomica Seed, Rhododendron Aureum Whole, Citrullus Colocynthis Whole, Solanum Dulcamara Whole, Kalmia Latifolia Whole, Magnesium Phosphate, Dibasic Trihydrate, Arsenic Trioxide, And Tribasic Calcium Phosphate
Substance Name:
Arnica Montana; Arsenic Trioxide; Black Cohosh; Bryonia Alba Whole; Causticum; Citrullus Colocynthis Whole; Ferrosoferric Phosphate; Kalmia Latifolia Whole; Magnesium Phosphate, Dibasic Trihydrate; Rhododendron Aureum Whole; Sodium Sulfate Anhydrous; Solanum Dulcamara Whole; Strychnos Nux-vomica Seed; Toxicodendron Pubescens Whole; Tribasic Calcium Phosphate
Usage Information:
This product is used as Muscular pain, stiffness, stress, fatigue.
11-Digit NDC Billing Format:
58264014001
Product Type:
Human Otc Drug
Labeler Name:
Dna Labs, Inc.
Dosage Form:
Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
Administration Route(s):
  • Sublingual - Administration beneath the tongue.
    • Active Ingredient(s):
  • ARNICA MONTANA 5 [hp_X]/mL
  • ARSENIC TRIOXIDE 8 [hp_X]/mL
  • BLACK COHOSH 3 [hp_X]/mL
  • BRYONIA ALBA WHOLE 4 [hp_X]/mL
  • CAUSTICUM 6 [hp_X]/mL
  • CITRULLUS COLOCYNTHIS WHOLE 6 [hp_X]/mL
  • FERROSOFERRIC PHOSPHATE 6 [hp_X]/mL
  • KALMIA LATIFOLIA WHOLE 6 [hp_X]/mL
  • MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 6 [hp_X]/mL
  • RHODODENDRON AUREUM WHOLE 6 [hp_X]/mL
  • SODIUM SULFATE ANHYDROUS 6 [hp_X]/mL
  • SOLANUM DULCAMARA WHOLE 6 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 6 [hp_X]/mL
  • TOXICODENDRON PUBESCENS WHOLE 4 [hp_X]/mL
  • TRIBASIC CALCIUM PHOSPHATE 8 [hp_X]/mL
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
  • Calcium - [CS]
  • Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
  • Cations, Divalent - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Increased Coagulation Factor Activity - [PE] (Physiologic Effect)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Increased IgG Production - [PE] (Physiologic Effect)
  • Increased Large Intestinal Motility - [PE] (Physiologic Effect)
  • Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Inhibition Small Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Magnesium Ion Exchange Activity - [MoA] (Mechanism of Action)
  • Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Osmotic Activity - [MoA] (Mechanism of Action)
  • Osmotic Laxative - [EPC] (Established Pharmacologic Class)
  • Plant Proteins - [CS]
  • Seed Storage Proteins - [CS]
  • Stimulation Large Intestine Fluid/Electrolyte Secretion - [PE] (Physiologic Effect)
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    01-01-1990
    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 58264-0140-1?

    The NDC Packaged Code 58264-0140-1 is assigned to a package of 29.57 ml in 1 bottle, glass of D134, a human over the counter drug labeled by Dna Labs, Inc.. The product's dosage form is solution and is administered via sublingual form.

    Is NDC 58264-0140 included in the NDC Directory?

    Yes, D134 with product code 58264-0140 is active and included in the NDC Directory. The product was first marketed by Dna Labs, Inc. on January 01, 1990 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 58264-0140-1?

    The 11-digit format is 58264014001. 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
    5-4-158264-0140-15-4-258264-0140-01