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  5. NDC Package Code: 43742-1325-4 Rheumagesic

NDC Package 43742-1325-4 Rheumagesic

Arnica Montana,Apis Mellifica,Benzoicum Acidum,Cartilago Suis,Ledum Palustre,Pantothenic - 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:
43742-1325-4
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
43742-1325
Proprietary Name:
Rheumagesic
Non-Proprietary Name:
Arnica Montana, Apis Mellifica, Benzoicum Acidum, Cartilago Suis, Ledum Palustre, Pantothenic Acid, Ruta Graveolens, Rhododendron Chrysanthum, Causticum, Formica Rufa, Sepia, Alpha-lipoicum Acidum, Aurum Metallicum, Calcarea Phosphorica, Colchicum Autumnale, Phytolacca Decandra, Radium Bromatum, Rhus Venenata, Thuja Occidentalis, Lac Caninum
Substance Name:
Apis Mellifera; Arnica Montana; Benzoic Acid; Canis Lupus Familiaris Milk; Causticum; Colchicum Autumnale Bulb; Formica Rufa; Gold; Pantothenic Acid; Phytolacca Americana Root; Radium Bromide; Rhododendron Aureum Leaf; Rhododendron Tomentosum Leafy Twig; Ruta Graveolens Flowering Top; Sepia Officinalis Juice; Sus Scrofa Cartilage; Thioctic Acid; Thuja Occidentalis Leafy Twig; Toxicodendron Vernix Leafy Twig; Tribasic Calcium Phosphate
Usage Information:
For temporary relief of symptoms related to arthritis including swelling, joint pain, back pain, inflammation in joints and muscle pain. ****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration. For temporary relief of symptoms related to arthritis including swelling, joint pain, back pain, inflammation in joints and muscle pain. ****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
11-Digit NDC Billing Format:
43742132504
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):
  • APIS MELLIFERA 6 [hp_X]/mL
  • ARNICA MONTANA 3 [hp_X]/mL
  • BENZOIC ACID 6 [hp_X]/mL
  • CANIS LUPUS FAMILIARIS MILK 16 [hp_X]/mL
  • CAUSTICUM 10 [hp_X]/mL
  • COLCHICUM AUTUMNALE BULB 12 [hp_X]/mL
  • FORMICA RUFA 10 [hp_X]/mL
  • GOLD 12 [hp_X]/mL
  • PANTOTHENIC ACID 6 [hp_X]/mL
  • PHYTOLACCA AMERICANA ROOT 12 [hp_X]/mL
  • RADIUM BROMIDE 12 [hp_X]/mL
  • RHODODENDRON AUREUM LEAF 8 [hp_X]/mL
  • RHODODENDRON TOMENTOSUM LEAFY TWIG 6 [hp_X]/mL
  • RUTA GRAVEOLENS FLOWERING TOP 6 [hp_X]/mL
  • SEPIA OFFICINALIS JUICE 10 [hp_X]/mL
  • SUS SCROFA CARTILAGE 6 [hp_X]/mL
  • THIOCTIC ACID 12 [hp_X]/mL
  • THUJA OCCIDENTALIS LEAFY TWIG 12 [hp_X]/mL
  • TOXICODENDRON VERNIX LEAFY TWIG 12 [hp_X]/mL
  • TRIBASIC CALCIUM PHOSPHATE 12 [hp_X]/mL
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Allergens - [CS]
  • Ammonium Ion Binding Activity - [MoA] (Mechanism of Action)
  • Bee Venoms - [CS]
  • Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
  • Calcium - [CS]
  • 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)
  • Nitrogen Binding Agent - [EPC] (Established Pharmacologic Class)
  • Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
  • Standardized Insect Venom Allergenic Extract - [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:
    01-09-2019
    End Marketing Date:
    10-08-2025
    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 43742-1325-4?

    The NDC Packaged Code 43742-1325-4 is assigned to a package of 30 ml in 1 bottle, dropper of Rheumagesic, 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 43742-1325 included in the NDC Directory?

    Yes, Rheumagesic with product code 43742-1325 is active and included in the NDC Directory. The product was first marketed by Deseret Biologicals, Inc. on January 09, 2019.

    What is the 11-digit format for NDC 43742-1325-4?

    The 11-digit format is 43742132504. 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
    5-4-143742-1325-45-4-243742-1325-04