Biochemic Tissue Salt Kit
NDC 85816-1201

Kit
Table of Contents
  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 85816-1201?
  5. Biochemic Tissue Salt Kit Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

Biochemic Tissue Salt Kit (cell salts) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Bm Private Limited. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a kit. This product entry covers the primary NDC 85816-1201 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
85816-1201
Proprietary Name:
Biochemic Tissue Salt Kit
Non-Proprietary Name: [1]
Cell Salts
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

Dosage Form:
Kit - A packaged collection of related material.

Labeler & Regulatory Data

Labeler Name: [5]
Bm Private Limited
Labeler Code:
85816
Product Label ID:
450e1d26-c1a8-dd79-e063-6394a90aa0e6
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
01-01-2015
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Product Characteristics

Color(s):
BM Kali Sulph (NDC 85816-1007): WHITE (C48325)
BM Mag Phos (NDC 85816-1008): WHITE (C48325)
BM Ferr Phos (NDC 85816-1004): WHITE (C48325)
BM Nat Mur (NDC 85816-1009): WHITE (C48325)
BM Nat Phos (NDC 85816-1010): WHITE (C48325)
BM Calc Fluor (NDC 85816-1001): WHITE (C48325)
BM Calc Phos (NDC 85816-1002): WHITE (C48325)
BM Kali Mur (NDC 85816-1005): WHITE (C48325)
BM Kali Phos (NDC 85816-1006): WHITE (C48325)
BM Nat Sulph (NDC 85816-1011): WHITE (C48325)
BM Silicea (NDC 85816-1012): WHITE (C48325)
BM Calc Sulph (NDC 85816-1003): WHITE (C48325)
Shape:
BM Kali Sulph (NDC 85816-1007): ROUND (C48348)
BM Mag Phos (NDC 85816-1008): ROUND (C48348)
BM Ferr Phos (NDC 85816-1004): ROUND (C48348)
BM Nat Mur (NDC 85816-1009): ROUND (C48348)
BM Nat Phos (NDC 85816-1010): ROUND (C48348)
BM Calc Fluor (NDC 85816-1001): ROUND (C48348)
BM Calc Phos (NDC 85816-1002): ROUND (C48348)
BM Kali Mur (NDC 85816-1005): ROUND (C48348)
BM Kali Phos (NDC 85816-1006): ROUND (C48348)
BM Nat Sulph (NDC 85816-1011): ROUND (C48348)
BM Silicea (NDC 85816-1012): ROUND (C48348)
BM Calc Sulph (NDC 85816-1003): ROUND (C48348)
Size(s):
BM Kali Sulph (NDC 85816-1007): 90 MM
BM Mag Phos (NDC 85816-1008): 90 MM
BM Ferr Phos (NDC 85816-1004): 90 MM
BM Nat Mur (NDC 85816-1009): 90 MM
BM Nat Phos (NDC 85816-1010): 90 MM
BM Calc Fluor (NDC 85816-1001): 90 MM
BM Calc Phos (NDC 85816-1002): 90 MM
BM Kali Mur (NDC 85816-1005): 90 MM
BM Kali Phos (NDC 85816-1006): 90 MM
BM Nat Sulph (NDC 85816-1011): 90 MM
BM Silicea (NDC 85816-1012): 90 MM
BM Calc Sulph (NDC 85816-1003): 90 MM
Score:
BM Kali Sulph (NDC 85816-1007): 1
BM Mag Phos (NDC 85816-1008): 1
BM Ferr Phos (NDC 85816-1004): 1
BM Nat Mur (NDC 85816-1009): 1
BM Nat Phos (NDC 85816-1010): 1
BM Calc Fluor (NDC 85816-1001): 1
BM Calc Phos (NDC 85816-1002): 1
BM Kali Mur (NDC 85816-1005): 1
BM Kali Phos (NDC 85816-1006): 1
BM Nat Sulph (NDC 85816-1011): 1
BM Silicea (NDC 85816-1012): 1
BM Calc Sulph (NDC 85816-1003): 1

Code Structure Chart

Product Details

What is NDC 85816-1201?

The NDC code 85816-1201 is assigned by the FDA to the product Biochemic Tissue Salt Kit. It is commonly known by its generic name, cell salts. This pharmaceutical product is labeled by Bm Private Limited and is currently categorized as listed product. The medication is a kit. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 85816-1201-1. 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?

Temporarily boost cellular nutrition, satisfy mineral imbalances in the body, and stimulate the body's natural healing process

Which are the associated UNII Codes?

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

  • BM Kali Sulph (NDC 85816-1007)
  • BM Mag Phos (NDC 85816-1008)
    • MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q)
    • MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
  • BM Ferr Phos (NDC 85816-1004)
    • FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7)
    • FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (Active Moiety)
  • BM Nat Mur (NDC 85816-1009)
  • BM Nat Phos (NDC 85816-1010)
    • SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE (UNII: 70WT22SF4B)
    • PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
  • BM Calc Fluor (NDC 85816-1001)
  • BM Calc Phos (NDC 85816-1002)
  • BM Kali Mur (NDC 85816-1005)
  • BM Kali Phos (NDC 85816-1006)
  • BM Nat Sulph (NDC 85816-1011)
  • BM Silicea (NDC 85816-1012)
  • BM Calc Sulph (NDC 85816-1003)

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:

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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 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 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".