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  4. NDC Product Code: 51720-653 Tyn Mans

NDC 51720-653 Tyn Mans

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 51720-653?
  5. Tyn Mans 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:
51720-653
Proprietary Name:
Tyn Mans
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Curative Power Lab Pvt Ltd
Labeler Code:
51720
Product Label ID:
46eb0c1f-aaef-4b73-b19f-af9a2baa7a81
Start Marketing Date: [9]
08-15-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
BROWN (C48332 - TRANSLUCENT BROWN)

Code Structure Chart

Product Details

What is NDC 51720-653?

The NDC code 51720-653 is assigned by the FDA to the product Tyn Mans which is product labeled by Curative Power Lab Pvt Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51720-653-26 1 bottle, plastic in 1 box / 100 ml in 1 bottle, plastic (51720-653-24). 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 Tyn Mans?

Tyn Man's. A homeopathic alternative. - Calms Inflammation- Soothes aching muscles- Eases arthritis painUses:Relieves pain from acute and chronic muscle or joint conditions such as arthritis, backache, gout, and bone or tendon injury.

Which are Tyn Mans UNII Codes?

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

Which are Tyn Mans 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:

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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".