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  4. NDC Product Code: 82437-020 Msm2000 Premium

NDC 82437-020 Msm2000 Premium

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 82437-020?
  5. Msm2000 Premium Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
82437-020
Proprietary Name:
Msm2000 Premium
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Vigen Medical
Labeler Code:
82437
Product Label ID:
06d7a21c-c318-4f97-802b-1889401b6288
Start Marketing Date: [9]
12-01-2021
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

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

Code Structure Chart

Product Details

What is NDC 82437-020?

The NDC code 82437-020 is assigned by the FDA to the product Msm2000 Premium which is product labeled by Vigen Medical. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 82437-020-02 120 blister pack in 1 carton / 506 mg in 1 blister pack (82437-020-01), 82437-020-03 360 blister pack in 1 carton / 506 mg in 1 blister pack (82437-020-01). 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 Msm2000 Premium?

■ Take 2 tablets twice a day with sufficient water.

Which are Msm2000 Premium UNII Codes?

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

Which are Msm2000 Premium 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:

* Please review the disclaimer below.

Product Footnotes

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

[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 ("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".