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  4. NDC Product Code: 70859-045 Dfs 1.5%/ms 25%/menth 6%/cap 0.025% Pak

NDC 70859-045 Dfs 1.5%/ms 25%/menth 6%/cap 0.025% Pak

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70859-045?
  4. Dfs 1.5%/ms 25%/menth 6%/cap 0.025% Pak Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
70859-045
Proprietary Name:
Dfs 1.5%/ms 25%/menth 6%/cap 0.025% Pak
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nucare Pharmaceuticals Inc
Labeler Code:
70859
Product Label ID:
7099d4b1-6893-234a-e053-2991aa0a682b
Start Marketing Date: [9]
07-29-2016
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 70859-045?

The NDC code 70859-045 is assigned by the FDA to the product Dfs 1.5%/ms 25%/menth 6%/cap 0.025% Pak which is product labeled by Nucare Pharmaceuticals Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70859-045-01 1 kit in 1 kit * 1 container in 1 carton (70859-028-03) / 90 ml in 1 container * 1 bottle in 1 carton (60505-0399-5) / 150 ml 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 Dfs 1.5%/ms 25%/menth 6%/cap 0.025% Pak?

Diclofenac sodium topical solution is a nonsteroidal anti-inflammatory drug (NSAID) indicated for the treatment of signs and symptoms of osteoarthritis of the knee(s).

Which are Dfs 1.5%/ms 25%/menth 6%/cap 0.025% Pak UNII Codes?

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

Which are Dfs 1.5%/ms 25%/menth 6%/cap 0.025% Pak 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:

What is the NDC to RxNorm Crosswalk for Dfs 1.5%/ms 25%/menth 6%/cap 0.025% Pak?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 1989491 - capsaicin 0.025 % / menthol 6 % / methyl salicylate 25 % Topical Solution
  • RxCUI: 1989491 - capsaicin 0.25 MG/ML / menthol 60 MG/ML / methyl salicylate 250 MG/ML Topical Solution
  • RxCUI: 857700 - diclofenac sodium 1.5 % Topical Solution
  • RxCUI: 857700 - diclofenac sodium 15 MG/ML Topical Solution
  • RxCUI: 857700 - diclofenac sodium 1.5 % (as diclofenac sodium 16.05 MG/ML) Topical Solution

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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".