NDC Package 43742-1592-1 Oral Health

Borax,Bryonia (alba),Echinacea Purpurea,Juglans Cinerea,Kali Muriaticum,Magnesia - View Billable Units, 11-Digit Format, RxNorm

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:
43742-1592-1
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
Proprietary Name:
Oral Health
Non-Proprietary Name:
Borax, Bryonia (alba), Echinacea Purpurea, Juglans Cinerea, Kali Muriaticum, Magnesia Muriatica, Muriaticum Acidum, Discus Intervertebralis Suis, Oral Mucosa (suis), Antimonium Crudum, Arsenicum Album, Bismuthum Subnitricum, Chamomilla, Cinchona Officinalis, Nux Moschata, Sambucus Nigra, Sepia, Mercurius Solubilis, Calcarea Phosphorica, Ignatia Amara, Oxygenium, Candida Albicans, Staphylococcus Aureus, Streptococcus Mutans
Substance Name:
Antimony Trisulfide; Arsenic Trioxide; Bismuth Subnitrate; Bryonia Alba Root; Candida Albicans; Cinchona Officinalis Bark; Echinacea Purpurea Whole; Hydrochloric Acid; Juglans Cinerea Branch Bark/root Bark; Magnesium Chloride; Matricaria Chamomilla Whole; Mercurius Solubilis; Nutmeg; Oxygen; Potassium Chloride; Sambucus Nigra Flowering Top; Sepia Officinalis Juice; Sodium Borate; Staphylococcus Aureus; Streptococcus Mutans; Strychnos Ignatii Seed; Sus Scrofa Intervertebral Disc; Sus Scrofa Oral Mucosa; Tribasic Calcium Phosphate
Usage Information:
For the temporary relief of symptoms related to oral health, such as cavitation, delayed dentition, dry mouth, painful eating, eruptions on tongue and inner cheeks and tooth sensitivity.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration. For the temporary relief of symptoms related to oral health, such as cavitation, delayed dentition, dry mouth, painful eating, eruptions on tongue and inner cheeks and tooth sensitivity.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
11-Digit NDC Billing Format:
43742159201
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.
  • Pharmacologic Class(es):
  • Allergens - [CS]
  • Allergens - [CS]
  • Bismuth - [CS]
  • Bismuth - [EPC] (Established Pharmacologic Class)
  • 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)
  • Dietary Proteins - [CS]
  • Food Additives - [CS]
  • Fungal Proteins - [CS]
  • 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 Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Non-Standardized Fungal Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Osmotic Activity - [MoA] (Mechanism of Action)
  • Osmotic Laxative - [EPC] (Established Pharmacologic Class)
  • Phosphate Binder - [EPC] (Established Pharmacologic Class)
  • Phosphate Chelating Activity - [MoA] (Mechanism of Action)
  • Plant Proteins - [CS]
  • Potassium Compounds - [CS]
  • Potassium Salt - [EPC] (Established Pharmacologic Class)
  • 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:
    02-19-2020
    End Marketing Date:
    09-19-2028
    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 43742-1592-1?

    The NDC Packaged Code 43742-1592-1 is assigned to a package of 30 ml in 1 bottle, dropper of Oral Health, 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 43742-1592 included in the NDC Directory?

    Yes, Oral Health with product code 43742-1592 is active and included in the NDC Directory. The product was first marketed by Deseret Biologicals, Inc. on February 19, 2020.

    What is the 11-digit format for NDC 43742-1592-1?

    The 11-digit format is 43742159201. 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
    5-4-143742-1592-15-4-243742-1592-01