Ringstop Tablet
NDC 70163-0003

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 70163-0003?
  5. Ringstop Uses
  6. Active Ingredients
  7. Active Ingredients UNII Codes
  8. Inactive Ingredients UNII Codes
  9. Pharmacologic Classes

Product Information

Ringstop (acetylsalicylicum acidum, calcarea carbonica, carbo vegetabilis, chininum sulphuricum, cimicifuga racemosa, cinchona officinalis, coffea cruda, graphites, kali carbonicum, lycopodium clavatum, natrum salicylicum) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Naturalcare. This medication is typically used as a allergens [cs]. It is supplied as a white tablet for oral administration. This product entry covers the primary NDC 70163-0003 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
70163-0003
Proprietary Name:
Ringstop
Non-Proprietary Name: [1]
Acetylsalicylicum Acidum, Calcarea Carbonica, Carbo Vegetabilis, Chininum Sulphuricum, Cimicifuga Racemosa, Cinchona Officinalis, Coffea Cruda, Graphites, Kali Carbonicum, Lycopodium Clavatum, Natrum Salicylicum
Substance Name: [2]
Activated Charcoal; Arabica Coffee Bean; Aspirin; Black Cohosh; Cinchona Officinalis Bark; Graphite; Lycopodium Clavatum Spore; Oyster Shell Calcium Carbonate, Crude; Potassium Carbonate; Quinine Sulfate; Sodium Salicylate
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

Dosage Form:
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.

Labeler & Regulatory Data

Labeler Name: [5]
Naturalcare
Labeler Code:
70163
Product Label ID:
f6e3501d-1a27-462d-ab07-1b2d6fe91535
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
03-02-2026
Listing Expiration Date: [11]
12-31-2027
Exclude Flag: [12]
N

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
10 MM
Imprint(s):
NC
Score:
1

Code Structure Chart

Product Details

What is NDC 70163-0003?

The NDC code 70163-0003 is assigned by the FDA to the product Ringstop. It is commonly known by its generic name, acetylsalicylicum acidum, calcarea carbonica, carbo vegetabilis, chininum sulphuricum, cimicifuga racemosa, cinchona officinalis, coffea cruda, graphites, kali carbonicum, lycopodium clavatum, natrum salicylicum. This pharmaceutical product is labeled by Naturalcare and is currently categorized as listed product. The medication is a tablet administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 70163-0003-1. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

Adults and children over the age of 12 :■ take 3 tablets per day for 3-90 days, then reduce to 1 tablet twice daily.

What are Active Ingredients of this product?

An 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.
  • ACTIVATED CHARCOAL 8 [hp_X]/1
  • ARABICA COFFEE BEAN 3 [hp_X]/1
  • ASPIRIN 6 [hp_X]/1 - The prototypical analgesic used in the treatment of mild to moderate pain. It has anti-inflammatory and antipyretic properties and acts as an inhibitor of cyclooxygenase which results in the inhibition of the biosynthesis of prostaglandins. Aspirin also inhibits platelet aggregation and is used in the prevention of arterial and venous thrombosis. (From Martindale, The Extra Pharmacopoeia, 30th ed, p5)
  • BLACK COHOSH 6 [hp_X]/1
  • CINCHONA OFFICINALIS BARK 12 [hp_X]/1
  • GRAPHITE 12 [hp_X]/1 - An allotropic form of carbon that is used in pencils, as a lubricant, and in matches and explosives. It is obtained by mining and its dust can cause lung irritation.
  • LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/1
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 8 [hp_X]/1
  • POTASSIUM CARBONATE 6 [hp_X]/1
  • QUININE SULFATE 12 [hp_X]/1 - An alkaloid derived from the bark of the cinchona tree. It is used as an antimalarial drug, and is the active ingredient in extracts of the cinchona that have been used for that purpose since before 1633. Quinine is also a mild antipyretic and analgesic and has been used in common cold preparations for that purpose. It was used commonly and as a bitter and flavoring agent, and is still useful for the treatment of babesiosis. Quinine is also useful in some muscular disorders, especially nocturnal leg cramps and myotonia congenita, because of its direct effects on muscle membrane and sodium channels. The mechanisms of its antimalarial effects are not well understood.
  • SODIUM SALICYLATE 6 [hp_X]/1 - A non-steroidal anti-inflammatory agent that is less effective than equal doses of ASPIRIN in relieving pain and reducing fever. However, individuals who are hypersensitive to ASPIRIN may tolerate sodium salicylate. In general, this salicylate produces the same adverse reactions as ASPIRIN, but there is less occult gastrointestinal bleeding. (From AMA Drug Evaluations Annual, 1992, p120)

Which are the associated UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are the Inactive Ingredients associated UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

Which are the Pharmacologic Classes of this product?

A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

* Please review the full disclaimer at the bottom of this page.

Product & Regulatory Definitions
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.
What is the Substance Name? An 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.
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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".