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  4. NDC Product Code: 84999-026 Schuessler Tissue Salts Comb D Skin Disorders

NDC 84999-026 Schuessler Tissue Salts Comb D Skin Disorders

Kali Muriaticum, Kali Sulphuricum, Calcarea Sulphurica, Silicea Tablet, Chewable Oral - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 84999-026?
  5. Schuessler Tissue Salts Comb D Skin Disorders Uses
  6. Active Ingredients
  7. Active Ingredients UNII Codes
  8. Inactive Ingredients UNII Codes
  9. Pharmacologic Classes

Product Information

Get all the details for National Drug Code (NDC) 84999-026 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
84999-026
Proprietary Name:
Schuessler Tissue Salts Comb D Skin Disorders
Non-Proprietary Name: [1]
Kali Muriaticum, Kali Sulphuricum, Calcarea Sulphurica, Silicea
Substance Name: [2]
Calcium Sulfate Dihydrate; Potassium Chloride; Potassium Sulfate; Silicon Dioxide
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Tablet, Chewable - A solid dosage form containing medicinal substances with or without suitable diluents that is intended to be chewed, producing a pleasant tasting residue in the oral cavity that is easily swallowed and does not leave a bitter or unpleasant after-taste.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.
Labeler Name: [5]
Martin & Pleasance Pty Ltd
Labeler Code:
84999
Product Label ID:
03153d92-dc68-4b84-a8c9-634b1ffd7da1
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
08-01-2025
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
OVAL (C48345)
Size(s):
12 MM
Score:
1

Code Structure Chart

Product Details

What is NDC 84999-026?

The NDC code 84999-026 is assigned by the FDA to the product Schuessler Tissue Salts Comb D Skin Disorders which is a human over the counter drug product labeled by Martin & Pleasance Pty Ltd. The generic name of Schuessler Tissue Salts Comb D Skin Disorders is kali muriaticum, kali sulphuricum, calcarea sulphurica, silicea. The product's dosage form is tablet, chewable and is administered via oral form. The product is distributed in a single package with assigned NDC code 84999-026-01 1 bottle in 1 carton / 125 tablet, chewable in 1 bottle. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Schuessler Tissue Salts Comb D Skin Disorders?

Use as directed Take 30 minutes away from food.Adults:  Acute dose: Chew 1 tablet every 30 minutes until symptoms subside, up to 6 times per day. Maintenance dose: Chew 1 tablet, 4 times daily. Children 6 years and older:   Acute dose: Crush ½ tablet, dissolve in water, and take every 30 minutes until symptoms subside, up to 6 times per day.Maintenance dose: Crush ½ tablet, dissolve in water, 4 times per day.

What are Schuessler Tissue Salts Comb D Skin Disorders Active Ingredients?

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.
  • CALCIUM SULFATE DIHYDRATE 6 [hp_X]/1 - A calcium salt that is used for a variety of purposes including: building materials, as a desiccant, in dentistry as an impression material, cast, or die, and in medicine for immobilizing casts and as a tablet excipient. It exists in various forms and states of hydration. Plaster of Paris is a mixture of powdered and heat-treated gypsum.
  • POTASSIUM CHLORIDE 6 [hp_X]/1 - A white crystal or crystalline powder used in BUFFERS; FERTILIZERS; and EXPLOSIVES. It can be used to replenish ELECTROLYTES and restore WATER-ELECTROLYTE BALANCE in treating HYPOKALEMIA.
  • POTASSIUM SULFATE 6 [hp_X]/1
  • SILICON DIOXIDE 6 [hp_X]/1 - Transparent, tasteless crystals found in nature as agate, amethyst, chalcedony, cristobalite, flint, sand, QUARTZ, and tridymite. The compound is insoluble in water or acids except hydrofluoric acid.

Which are Schuessler Tissue Salts Comb D Skin Disorders UNII Codes?

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

Which are Schuessler Tissue Salts Comb D Skin Disorders Inactive Ingredients 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 for Schuessler Tissue Salts Comb D Skin Disorders?

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Product Footnotes

[1] 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.

[2] 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.

[3] 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.

[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

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

[8] 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.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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".