1. Home
  2. Labeler Index
  3. Deseret Biologicals, Inc.
  4. 43742-0660
  5. NDC Package Code: 43742-0660-1 Arthritis Joints

NDC Package 43742-0660-1 Arthritis Joints

Gnaphalium Polycephalum,Berberis Vulgaris,Cimicifuga Racemosa,Cinchona - 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:
43742-0660-1
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
43742-0660
Proprietary Name:
Arthritis Joints
Non-Proprietary Name:
Gnaphalium Polycephalum, Berberis Vulgaris, Cimicifuga Racemosa, Cinchona Officinalis, Colocynthis, Ledum Palustre, Ranunculus Bulbosus, Aesculus Hippocastanum, Borax, Cuprum Aceticum, Kali Carbonicum, Pulsatilla (vulgaris), Secale Cornutum, Ammonium Muriaticum, Silicea, Argentum Metallicum, Calcarea Phosphorica, Glandula Suprarenalis Suis, Mercurius Praecipitatus Ruber, Sepia, Zincum Metallicum, Palladium Metallicum, Picricum Acidum, Sulphur, Cartilago Suis, Intervertebral Disc (suis), Medulla Ossis Suis
Substance Name:
Ammonium Chloride; Berberis Vulgaris Root Bark; Black Cohosh; Cinchona Officinalis Bark; Citrullus Colocynthis Fruit Pulp; Claviceps Purpurea Sclerotium; Cupric Acetate; Horse Chestnut; Ledum Palustre Twig; Mercuric Oxide; Palladium; Picric Acid; Potassium Carbonate; Pseudognaphalium Obtusifolium; Pulsatilla Vulgaris; Ranunculus Bulbosus; Sepia Officinalis Juice; Silicon Dioxide; Silver; Sodium Borate; Sulfur; Sus Scrofa Adrenal Gland; Sus Scrofa Bone Marrow; Sus Scrofa Cartilage; Sus Scrofa Intervertebral Disc; Tribasic Calcium Phosphate; Zinc
Usage Information:
For temporary relief of symptoms related to arthritis, including rash, itching, numbness and tingling, stress and anxiety, headache, fatigue, swelling, and joint pain.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration. For temporary relief of symptoms related to arthritis, including rash, itching, numbness and tingling, stress and anxiety, headache, fatigue, swelling, and joint pain.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.
11-Digit NDC Billing Format:
43742066001
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):
  • AMMONIUM CHLORIDE 8 [hp_X]/mL
  • BERBERIS VULGARIS ROOT BARK 4 [hp_X]/mL
  • BLACK COHOSH 4 [hp_X]/mL
  • CINCHONA OFFICINALIS BARK 4 [hp_X]/mL
  • CITRULLUS COLOCYNTHIS FRUIT PULP 4 [hp_X]/mL
  • CLAVICEPS PURPUREA SCLEROTIUM 6 [hp_X]/mL
  • CUPRIC ACETATE 6 [hp_X]/mL
  • HORSE CHESTNUT 6 [hp_X]/mL
  • LEDUM PALUSTRE TWIG 4 [hp_X]/mL
  • MERCURIC OXIDE 10 [hp_X]/mL
  • PALLADIUM 12 [hp_X]/mL
  • PICRIC ACID 12 [hp_X]/mL
  • POTASSIUM CARBONATE 6 [hp_X]/mL
  • PSEUDOGNAPHALIUM OBTUSIFOLIUM 3 [hp_X]/mL
  • PULSATILLA VULGARIS 6 [hp_X]/mL
  • RANUNCULUS BULBOSUS 4 [hp_X]/mL
  • SEPIA OFFICINALIS JUICE 10 [hp_X]/mL
  • SILICON DIOXIDE 8 [hp_X]/mL
  • SILVER 10 [hp_X]/mL
  • SODIUM BORATE 6 [hp_X]/mL
  • SULFUR 30 [hp_X]/mL
  • SUS SCROFA ADRENAL GLAND 10 [hp_X]/mL
  • SUS SCROFA BONE MARROW 12 [hp_X]/mL
  • SUS SCROFA CARTILAGE 12 [hp_X]/mL
  • SUS SCROFA INTERVERTEBRAL DISC 12 [hp_X]/mL
  • TRIBASIC CALCIUM PHOSPHATE 10 [hp_X]/mL
  • ZINC 10 [hp_X]/mL
    • Pharmacologic Class(es):
  • Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
  • Calcium - [CS]
  • Cations, Divalent - [CS]
  • Increased Coagulation Factor Activity - [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:
    11-11-2015
    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 43742-0660-1?

    The NDC Packaged Code 43742-0660-1 is assigned to a package of 30 ml in 1 bottle, dropper of Arthritis Joints, 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 43742-0660 included in the NDC Directory?

    Yes, Arthritis Joints with product code 43742-0660 is active and included in the NDC Directory. The product was first marketed by Deseret Biologicals, Inc. on November 11, 2015 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 43742-0660-1?

    The 11-digit format is 43742066001. 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
    5-4-143742-0660-15-4-243742-0660-01