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  5. NDC Package Code: 43742-1201-1 Focus

NDC Package 43742-1201-1 Focus

Ginkgo Biloba,Alpha-ketoglutaricum Acidum,Iodium,Phosphorus,Sarcolacticum Acid,Saccharum - 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:
43742-1201-1
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
43742-1201
Proprietary Name:
Focus
Non-Proprietary Name:
Ginkgo Biloba, Alpha-ketoglutaricum Acidum, Iodium, Phosphorus, Sarcolacticum Acid, Saccharum Officinale, Adenosinum Cyclophosphoricum, Cerebrum Suis, Hypothalamus Suis, Silicea, Adrenalinum, Ambra Grisea, Carboneum Sulphuratum, Tarentula Hispana, Aethusa Cynapium, Baryta Carbonica, Helleborus Niger, Veratrum Album, Candida Albicans, Hyoscyamus Niger
Substance Name:
Adenosine Cyclic Phosphate; Aethusa Cynapium; Ambergris; Barium Carbonate; Candida Albicans; Carbon Disulfide; Epinephrine; Ginkgo; Helleborus Niger Root; Hyoscyamus Niger; Iodine; Lactic Acid, L-; Lycosa Tarantula; Oxogluric Acid; Phosphorus; Silicon Dioxide; Sucrose; Sus Scrofa Cerebrum; Sus Scrofa Hypothalamus; Veratrum Album Root
Usage Information:
For temporary relief of symptoms due to various deficit disorders and hyperactivity, such as difficult concentration, impulsivity, restlessness, temper tantrums, quick temper, easily bored, forgetful, noise sensitivity, and mood changes.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration. For temporary relief of symptoms due to various deficit disorders and hyperactivity, such as difficult concentration, impulsivity, restlessness, temper tantrums, quick temper, easily bored, forgetful, noise sensitivity, and mood changes.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
11-Digit NDC Billing Format:
43742120101
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):
  • ADENOSINE CYCLIC PHOSPHATE 8 [hp_X]/mL
  • AETHUSA CYNAPIUM 12 [hp_X]/mL
  • AMBERGRIS 9 [hp_X]/mL
  • BARIUM CARBONATE 12 [hp_X]/mL
  • CANDIDA ALBICANS 12 [hp_X]/mL
  • CARBON DISULFIDE 9 [hp_X]/mL
  • EPINEPHRINE 8 [hp_X]/mL
  • GINKGO 3 [hp_X]/mL
  • HELLEBORUS NIGER ROOT 12 [hp_X]/mL
  • HYOSCYAMUS NIGER 12 [hp_X]/mL
  • IODINE 6 [hp_X]/mL
  • LACTIC ACID, L- 6 [hp_X]/mL
  • LYCOSA TARANTULA 10 [hp_X]/mL
  • OXOGLURIC ACID 6 [hp_X]/mL
  • PHOSPHORUS 6 [hp_X]/mL
  • SILICON DIOXIDE 8 [hp_X]/mL
  • SUCROSE 6 [hp_X]/mL
  • SUS SCROFA CEREBRUM 8 [hp_X]/mL
  • SUS SCROFA HYPOTHALAMUS 8 [hp_X]/mL
  • VERATRUM ALBUM ROOT 12 [hp_X]/mL
    • Pharmacologic Class(es):
  • Adrenergic alpha-Agonists - [MoA] (Mechanism of Action)
  • Adrenergic beta-Agonists - [MoA] (Mechanism of Action)
  • Allergens - [CS]
  • Catecholamine - [EPC] (Established Pharmacologic Class)
  • Catecholamines - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Fungal Proteins - [CS]
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Increased IgG Production - [PE] (Physiologic Effect)
  • Non-Standardized Fungal Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • alpha-Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
  • beta-Adrenergic Agonist - [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:
    05-24-2018
    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 43742-1201-1?

    The NDC Packaged Code 43742-1201-1 is assigned to a package of 30 ml in 1 bottle, dropper of Focus, 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 43742-1201 included in the NDC Directory?

    Yes, Focus with product code 43742-1201 is active and included in the NDC Directory. The product was first marketed by Deseret Biologicals, Inc. on May 24, 2018 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 43742-1201-1?

    The 11-digit format is 43742120101. 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
    5-4-143742-1201-15-4-243742-1201-01