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  4. NDC Product Code: 70253-153 Dandruff

NDC 70253-153 Dandruff

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70253-153?
  4. Dandruff Uses
  5. Active 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:
70253-153
Proprietary Name:
Dandruff
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nash Finch Company
Labeler Code:
70253
Product Label ID:
f44680c8-2fa1-42fc-80fb-fa5d89ce97e9
Start Marketing Date: [9]
06-05-1998
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 70253-153-15

Package Description: 420 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 70253-153?

The NDC code 70253-153 is assigned by the FDA to the product Dandruff which is product labeled by Nash Finch Company. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70253-153-15 420 ml in 1 bottle, plastic . 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 Dandruff?

Use helps prevent recurrence of flaking and itching associated with dandruff.

Which are Dandruff UNII Codes?

The UNII codes for the active 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".