NDC 62795-1128 Hendel Schuessler Cell Salts

Calcium Fluoride, Tribasic Calcium Phosphate, Calcium Sulfate Anhydrous, Ferrous Phosphate, Potassium Chloride, Potassium Sulfate, Magnesium Phosphate, Dibasic, Sodium Phosphate, Dibasic, Sodium Sulfate And Silicon Dioxide

NDC Product Code 62795-1128

NDC CODE: 62795-1128

Proprietary Name: Hendel Schuessler Cell Salts 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: Calcium Fluoride, Tribasic Calcium Phosphate, Calcium Sulfate Anhydrous, Ferrous Phosphate, Potassium Chloride, Potassium Sulfate, Magnesium Phosphate, Dibasic, Sodium Phosphate, Dibasic, Sodium Sulfate And Silicon Dioxide 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

  • 62795 - Medinatura Inc

NDC 62795-1128-2

Package Description: 100 TABLET in 1 BOTTLE

NDC Product Information

Hendel Schuessler Cell Salts with NDC 62795-1128 is a a human over the counter drug product labeled by Medinatura Inc. The generic name of Hendel Schuessler Cell Salts is calcium fluoride, tribasic calcium phosphate, calcium sulfate anhydrous, ferrous phosphate, potassium chloride, potassium sulfate, magnesium phosphate, dibasic, sodium phosphate, dibasic, sodium sulfate and silicon dioxide. The product's dosage form is tablet and is administered via oral form.

Dosage Form: Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.

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.

Hendel Schuessler Cell Salts 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.

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.


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: Medinatura Inc
Labeler Code: 62795
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: 08-16-2016 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: 12-31-2022 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 - NO 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Hendel Schuessler Cell Salts Product Label Images

Hendel Schuessler Cell Salts 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


If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If symptoms persist or worsen, a health professional should be consulted. Do not use if sensitivity to Schuessler Cell Salts or any of its ingredients exists. In case of accidental overdose, contact a Poison Control Center immediately.

Keep Out Of Reach Of Children



Promotes Healthy cell Function


Each tablet contains equal parts of Calcarea fluorica 6X, Calcarea phosphorica 6X, Calcarea sulphurica 6X, Ferrum phoshporicum 6X, Kali muriatcum 6X, Kali phosphoricum 6X, Kali sulphuricum 6X, Magnesia phosphorica 6X, Natrum muriaticum 6X, Natrum phosphoricum 6X, Natrum sulphuricum 6X, Silicea 6X.

Inactive Ingredient

Lactose, Magnesium stearate


Adults 18 and over: 1 tablet sublingually or dissolved completely in mouth 2 to 3 times per day or as directed by a physician


For the temporary relief of:• Promotes Healthy cell Function

* Please review the disclaimer below.