55714-2551 NDC - RHEUMATIC-JOINT CARE (URICUM ACIDUM, ACONITUM NAP.,APIS MEL., ARNICA, ARSENICUM ALB, BELLADONNA,BENZOICUM ACIDUM, BRYONIA, CALC. CARB., CHAMOMILLA, CINCHONA, COLCHICUM, EUPATORIUM PERF., GAULTHERIAPROCUMBENS, GUAIACUM, IODIUM, KALI BIC, KALMIA,LEDUM, PULSATILLA, RHUS TOXICODENDRON, RUTA,SABINA, STRYCHNINUM, LAPPA, PHYTOLACCA, SYMPHYTUM,)

Drug Information

  • Product NDC: 55714-2551
  • Proprietary Name: Rheumatic-Joint Care
  • Non Proprietary Name: Uricum acidum, Aconitum nap.,Apis mel., Arnica, Arsenicum alb, Belladonna,Benzoicum acidum, Bryonia, Calc. carb., Chamomilla, Cinchona, Colchicum, Eupatorium perf., Gaultheriaprocumbens, Guaiacum, Iodium, Kali bic, Kalmia,Ledum, Pulsatilla, Rhus toxicodendron, Ruta,Sabina, Strychninum, Lappa, Phytolacca, Symphytum,
  • Active Ingredient(s): 15 [hp_X]/g ACONITUM NAPELLUS; 15 [hp_X]/g ANEMONE PULSATILLA; 15 [hp_X]/g APIS MELLIFERA; 6 [hp_X]/g ARCTIUM LAPPA ROOT; 15 [hp_X]/g ARNICA MONTANA; 15 [hp_X]/g ARSENIC TRIOXIDE; 15 [hp_X]/g ATROPA BELLADONNA; 15 [hp_X]/g BENZOIC ACID; 15 [hp_X]/g BRYONIA ALBA ROOT; 15 [hp_X]/g CINCHONA OFFICINALIS BARK; 15 [hp_X]/g COLCHICUM AUTUMNALE BULB; 6 [hp_X]/g COMFREY ROOT; 15 [hp_X]/g EUPATORIUM PERFOLIATUM FLOWERING TOP; 15 [hp_X]/g GAULTHERIA PROCUMBENS TOP; 15 [hp_X]/g GUAIACUM OFFICINALE RESIN; 15 [hp_X]/g IODINE; 15 [hp_X]/g JUNIPERUS SABINA LEAFY TWIG; 15 [hp_X]/g KALMIA LATIFOLIA LEAF; 15 [hp_X]/g MATRICARIA CHAMOMILLA; 15 [hp_X]/g OYSTER SHELL CALCIUM CARBONATE, CRUDE; 6 [hp_X]/g PHYTOLACCA AMERICANA ROOT; 15 [hp_X]/g POTASSIUM DICHROMATE; 15 [hp_X]/g RHODODENDRON TOMENTOSUM LEAFY TWIG; 15 [hp_X]/g RUTA GRAVEOLENS FLOWERING TOP; 15 [hp_X]/g STRYCHNINE; 15 [hp_X]/g TOXICODENDRON PUBESCENS LEAF; 15 [hp_X]/g URIC ACID
  • Administration Route(s): ORAL
  • Dosage Form(s): PELLET
  • Pharmacy Class(es): Allergens [CS]; Ammonium Ion Binding Activity [MoA]; Bee Venoms [CS]; Cell-mediated Immunity [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Nitrogen Binding Agent [EPC]; Standardized Insect Venom Allergenic Extract [EPC]

Labeler Information

Field Name Field Value
Labeler Name: Newton Laboratories, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:7/1/2019

Package Information

No. Package Code Package Description Billing Unit
155714-2551-128 g in 1 BOTTLE, GLASS (55714-2551-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC55714-2551This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
PRODUCT TYPE NAMEHUMAN OTC DRUGProduct 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.
PROPRIETARY NAMERheumatic-Joint CareThis corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
NON PROPRIETARY NAMEUricum acidum, Aconitum nap.,Apis mel., Arnica, Arsenicum alb, Belladonna,Benzoicum acidum, Bryonia, Calc. carb., Chamomilla, Cinchona, Colchicum, Eupatorium perf., Gaultheriaprocumbens, Guaiacum, Iodium, Kali bic, Kalmia,Ledum, Pulsatilla, Rhus toxicodendron, Ruta,Sabina, Strychninum, Lappa, Phytolacca, Symphytum,Name of Company corresponding to the labeler code segment of the Product NDC.
DOSAGE FORM NAMEPELLETThe 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 DATE7/1/2019This 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 NAMENewton Laboratories, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEACONITUM NAPELLUS; ANEMONE PULSATILLA; APIS MELLIFERA; ARCTIUM LAPPA ROOT; ARNICA MONTANA; ARSENIC TRIOXIDE; ATROPA BELLADONNA; BENZOIC ACID; BRYONIA ALBA ROOT; CINCHONA OFFICINALIS BARK; COLCHICUM AUTUMNALE BULB; COMFREY ROOT; EUPATORIUM PERFOLIATUM FLOWERING TOP; GAULTHERIA PROCUMBENS TOP; GUAIACUM OFFICINALE RESIN; IODINE; JUNIPERUS SABINA LEAFY TWIG; KALMIA LATIFOLIA LEAF; MATRICARIA CHAMOMILLA; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHYTOLACCA AMERICANA ROOT; POTASSIUM DICHROMATE; RHODODENDRON TOMENTOSUM LEAFY TWIG; RUTA GRAVEOLENS FLOWERING TOP; STRYCHNINE; TOXICODENDRON PUBESCENS LEAF; URIC ACIDAn 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 STRENGTH15; 15; 15; 6; 15; 15; 15; 15; 15; 15; 15; 6; 15; 15; 15; 15; 15; 15; 15; 15; 6; 15; 15; 15; 15; 15; 15 
ACTIVE INGRED UNIT[hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g 
PHARM CLASSESAllergens [CS], Ammonium Ion Binding Activity [MoA], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Nitrogen Binding Agent [EPC], Standardized Insect Venom Allergenic Extract [EPC] 

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This page was last updated on: 11/21/2025

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