NDC 55714-2217 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,

NDC Product Code 55714-2217

NDC Code: 55714-2217

Proprietary Name: Rheumatic - Joint Care What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

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, What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 55714 - Newton Laboratories, Inc.
    • 55714-2217 - Rheumatic - Joint Care

NDC 55714-2217-0

Package Description: 7.08 g in 1 BOTTLE, GLASS

NDC 55714-2217-1

Package Description: 28.35 g in 1 BOTTLE, GLASS

NDC 55714-2217-2

Package Description: 56.7 g in 1 BOTTLE, GLASS

NDC Product Information

Rheumatic - Joint Care with NDC 55714-2217 is a a human over the counter drug product labeled by Newton Laboratories, Inc.. The generic name of Rheumatic - Joint Care is 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,. The product's dosage form is pellet and is administered via oral form.

Labeler Name: Newton Laboratories, Inc.

Dosage Form: Pellet - A small sterile solid mass consisting of a highly purified drug (with or without excipients) made by the formation of granules, or by compression and molding.

Product Type: Human Otc Drug What kind of product is this?
Indicates 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.

Rheumatic - Joint Care Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • URIC ACID 15 [hp_X]/g
  • ACONITUM NAPELLUS 10 [hp_X]/g
  • APIS MELLIFERA 10 [hp_X]/g
  • ARNICA MONTANA 10 [hp_X]/g
  • ARSENIC TRIOXIDE 10 [hp_X]/g
  • ATROPA BELLADONNA 10 [hp_X]/g
  • BENZOIC ACID 10 [hp_X]/g
  • BRYONIA ALBA ROOT 10 [hp_X]/g
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 10 [hp_X]/g
  • MATRICARIA RECUTITA 10 [hp_X]/g
  • CINCHONA OFFICINALIS BARK 10 [hp_X]/g
  • COLCHICUM AUTUMNALE BULB 10 [hp_X]/g
  • EUPATORIUM PERFOLIATUM FLOWERING TOP 10 [hp_X]/g
  • GAULTHERIA PROCUMBENS TOP 10 [hp_X]/g
  • GUAIACUM OFFICINALE RESIN 10 [hp_X]/g
  • IODINE 10 [hp_X]/g
  • POTASSIUM DICHROMATE 10 [hp_X]/g
  • KALMIA LATIFOLIA LEAF 10 [hp_X]/g
  • LEDUM PALUSTRE TWIG 10 [hp_X]/g
  • PULSATILLA VULGARIS 10 [hp_X]/g
  • TOXICODENDRON PUBESCENS LEAF 10 [hp_X]/g
  • RUTA GRAVEOLENS FLOWERING TOP 10 [hp_X]/g
  • JUNIPERUS SABINA LEAFY TWIG 10 [hp_X]/g
  • STRYCHNINE 10 [hp_X]/g
  • ARCTIUM LAPPA ROOT 3 [hp_X]/g
  • PHYTOLACCA AMERICANA ROOT 3 [hp_X]/g
  • COMFREY ROOT 3 [hp_X]/g

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • SUCROSE (UNII: C151H8M554)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Newton Laboratories, Inc.
Labeler Code: 55714
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product 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.

Start Marketing Date: 03-01-2011 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2019 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Rheumatic - Joint Care Product Label Images

Rheumatic - Joint Care Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Indications & Usage Section

Rheumatic - Joint Care  Formulated for symptoms associated with uric acid build-up such as joint pain, inflammation and discomfort.

Dosage & Administration Section

Directions:  Ages 12 and up, take 6 pellets orally (ages 0 to 11, give 3 pellets) one to four times daily or as directed by a healthcare professional. Under age 2, crush or dissolve pellets in purified water.  Sensitive persons begin with 1 pellet and gradually increase to full dose.

Otc - Active Ingredient Section

Uricum acidum 15x, Aconitum nap. 10x, Apis mel. 10x, Arnica 10x, Arsenicum alb. 10x, Belladonna 10x, Benzoicum acidum 10x, Bryonia 10x, Calc. carb. 10x, Chamomilla 10x, Cinchona 10x, Colchicum 10x, Eupatorium perf. 10x, Gaultheria procumbens 10x, Guaiacum 10x, Iodium 10x, Kali bic. 10x, Kalmia 10x, Ledum 10x, Pulsatilla 10x, Rhus toxicodendron 10x, Ruta 10x, Sabina 10x, Strychninum 10x, Lappa 3x, Phytolacca 3x, Symphytum 3x.

Otc - Purpose Section

Formulated for symptoms associated with uric acid build-up such as joint pain, inflammation and discomfort.

Inactive Ingredient Section

Inactive Ingredients: Gluten-free, non-GMO, beet-derived sucrose pellets.

Questions Section

Www.newtonlabs.net Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30012Questions?  1.800.448.7256

Warnings Section

Warning: Do not use if tamper - evident seal is broken or missing. Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days. Keep out of reach of children

Otc - Pregnancy Or Breast Feeding Section

Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days.

Otc - Keep Out Of Reach Of Children Section

Keep out of reach of children.

* Please review the disclaimer below.

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