43742-0660 NDC - ARTHRITIS JOINTS (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)

Drug Information

Product NDC: 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

Active Ingredient(s):
  • 8 [hp_X]/mL AMMONIUM CHLORIDE;
  • 4 [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;
  • 6 [hp_X]/mL CLAVICEPS PURPUREA SCLEROTIUM;
  • 6 [hp_X]/mL CUPRIC ACETATE;
  • 6 [hp_X]/mL HORSE CHESTNUT;
  • 4 [hp_X]/mL LEDUM PALUSTRE TWIG;
  • 10 [hp_X]/mL MERCURIC OXIDE;
  • 12 [hp_X]/mL PALLADIUM;
  • 12 [hp_X]/mL PICRIC ACID;
  • 6 [hp_X]/mL POTASSIUM CARBONATE;
  • 3 [hp_X]/mL PSEUDOGNAPHALIUM OBTUSIFOLIUM;
  • 6 [hp_X]/mL PULSATILLA VULGARIS;
  • 4 [hp_X]/mL RANUNCULUS BULBOSUS;
  • 10 [hp_X]/mL SEPIA OFFICINALIS JUICE;
  • 8 [hp_X]/mL SILICON DIOXIDE;
  • 10 [hp_X]/mL SILVER;
  • 6 [hp_X]/mL SODIUM BORATE;
  • 30 [hp_X]/mL SULFUR;
  • 10 [hp_X]/mL SUS SCROFA ADRENAL GLAND;
  • 12 [hp_X]/mL SUS SCROFA BONE MARROW;
  • 12 [hp_X]/mL SUS SCROFA CARTILAGE;
  • 12 [hp_X]/mL SUS SCROFA INTERVERTEBRAL DISC;
  • 10 [hp_X]/mL TRIBASIC CALCIUM PHOSPHATE;
  • 10 [hp_X]/mL ZINC


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Blood Coagulation Factor [EPC];
  • Calcium [CS];
  • Cations;
  • Divalent [CS];
  • Increased Coagulation Factor Activity [PE]

Labeler Information

Labeler Name: Deseret Biologicals, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:11/11/2015

Package Information

No. Package Code Package Description Billing Unit
143742-0660-130 mL in 1 BOTTLE, DROPPER (43742-0660-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43742-0660The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMEArthritis JointsThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEGnaphalium 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 SuisThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE11/11/2015This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMEDeseret Biologicals, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEAMMONIUM 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; ZINCAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH8; 4; 4; 4; 4; 6; 6; 6; 4; 10; 12; 12; 6; 3; 6; 4; 10; 8; 10; 6; 30; 10; 12; 12; 12; 10; 10 
ACTIVE INGRED UNIT[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL 
PHARM CLASSESBlood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE] 

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This page was last updated on: 2/1/2023