1. Home
  2. Labeler Index
  3. Deseret Biologicals, Inc.
  4. 43742-2120
  5. NDC Package Code: 43742-2120-1 Dysbio Plus

NDC Package 43742-2120-1 Dysbio Plus

Aceticum Acidum,Aloe,Arsenicum Album,Botulinum,Brugia Malayi,Chininum Sulphuricum,Cholera - 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:
43742-2120-1
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
43742-2120
Proprietary Name:
Dysbio Plus
Non-Proprietary Name:
Aceticum Acidum, Aloe, Arsenicum Album, Botulinum, Brugia Malayi, Chininum Sulphuricum, Cholera Nosode, Clostridium Difficile, Colchicum Autumnale, Colibacillinum Cum Natrum Muriaticum, Colocynthis, Echinacea (angustifolia), Helicobacter Pylori, Helicobacter Pylori Dna, Mercurius Corrosivus, Morgan Gaertner, Nux Vomica, Proteus (vulgaris), Salmonella Typhi Nosode
Substance Name:
Acetic Acid; Aloe; Arsenic Trioxide; Brugia Malayi; Citrullus Colocynthis Fruit Pulp; Clostridium Botulinum; Clostridium Difficile; Colchicum Autumnale Bulb; Echinacea Angustifolia Whole; Escherichia Coli; Helicobacter Pylori; Helicobacter Pylori Dna; Mercuric Chloride; Proteus Vulgaris; Quinine Sulfate; Salmonella Enterica Enterica Serovar Enteritidis; Salmonella Enterica Enterica Serovar Typhi; Strychnos Nux-vomica Seed; Vibrio Cholerae
Usage Information:
1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.
11-Digit NDC Billing Format:
43742212001
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.
    • Active Ingredient(s):
  • ACETIC ACID 12 [hp_X]/mL
  • ALOE 7 [hp_X]/mL
  • ARSENIC TRIOXIDE 8 [hp_X]/mL
  • BRUGIA MALAYI 39 [hp_C]/mL
  • CITRULLUS COLOCYNTHIS FRUIT PULP 8 [hp_X]/mL
  • CLOSTRIDIUM BOTULINUM 30 [hp_X]/mL
  • CLOSTRIDIUM DIFFICILE 30 [hp_C]/mL
  • COLCHICUM AUTUMNALE BULB 8 [hp_X]/mL
  • ECHINACEA ANGUSTIFOLIA WHOLE 3 [hp_X]/mL
  • ESCHERICHIA COLI 30 [hp_X]/mL
  • HELICOBACTER PYLORI 30 [hp_X]/mL
  • HELICOBACTER PYLORI DNA 16 [hp_X]/mL
  • MERCURIC CHLORIDE 8 [hp_X]/mL
  • PROTEUS VULGARIS 16 [hp_X]/mL
  • QUININE SULFATE 12 [hp_X]/mL
  • SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS 30 [hp_C]/mL
  • SALMONELLA ENTERICA ENTERICA SEROVAR TYPHI 33 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 8 [hp_X]/mL
  • VIBRIO CHOLERAE 16 [hp_X]/mL
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Antimalarial - [EPC] (Established Pharmacologic Class)
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Increased IgG Production - [PE] (Physiologic Effect)
  • 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:
    02-07-2024
    Listing Expiration Date:
    12-31-2025
    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 43742-2120-1?

    The NDC Packaged Code 43742-2120-1 is assigned to a package of 30 ml in 1 bottle, dropper of Dysbio Plus, 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 43742-2120 included in the NDC Directory?

    Yes, Dysbio Plus with product code 43742-2120 is active and included in the NDC Directory. The product was first marketed by Deseret Biologicals, Inc. on February 07, 2024 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 43742-2120-1?

    The 11-digit format is 43742212001. 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
    5-4-143742-2120-15-4-243742-2120-01