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  4. NDC Product Code: 13925-506 Fluocinolone Acetonide

NDC 13925-506 Fluocinolone Acetonide

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 13925-506?
  4. Fluocinolone Acetonide Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk
  8. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
13925-506
Proprietary Name:
Fluocinolone Acetonide
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Seton Pharmaceuticals
Labeler Code:
13925
Product Label ID:
bd2fe552-f27c-4a54-89f4-6825fdf5a4d2
Start Marketing Date: [9]
08-20-2013
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 13925-506-04

Package Description: 1 BOTTLE in 1 CARTON / 118.28 mL in 1 BOTTLE

Price per Unit: $0.72898 per ML

Product Details

What is NDC 13925-506?

The NDC code 13925-506 is assigned by the FDA to the product Fluocinolone Acetonide which is product labeled by Seton Pharmaceuticals. The product's dosage form is . The product is distributed in a single package with assigned NDC code 13925-506-04 1 bottle in 1 carton / 118.28 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 Fluocinolone Acetonide?

This medication is used to treat a variety of skin conditions (e.g., eczema, dermatitis, allergies, rash). Fluocinolone reduces the swelling, itching, and redness that can occur in these types of conditions. This medication is a medium-strength corticosteroid.

Which are Fluocinolone Acetonide UNII Codes?

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

  • FLUOCINOLONE ACETONIDE (UNII: 0CD5FD6S2M)
  • FLUOCINOLONE ACETONIDE (UNII: 0CD5FD6S2M) (Active Moiety)

Which are Fluocinolone Acetonide 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 Fluocinolone Acetonide?

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:

* Please review the disclaimer below.

Patient Education

Fluocinolone Topical


Fluocinolone topical is used to treat the itching, redness, dryness, crusting, scaling, inflammation, and discomfort of various skin conditions, including psoriasis (a skin disease in which red, scaly patches form on some areas of the body and eczema (a skin disease that causes the skin to be dry and itchy and to sometimes develop red, scaly rashes). Fluocinolone is in a class of medications called corticosteroids. It works by activating natural substances in the skin to reduce swelling, redness, and itching.
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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".