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  4. NDC Product Code: 41520-718 Careone Medicated Dandruff With Menthol

NDC 41520-718 Careone Medicated Dandruff With Menthol

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 41520-718?
  4. Careone Medicated Dandruff With Menthol 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:
41520-718
Proprietary Name:
Careone Medicated Dandruff With Menthol
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
American Sales Company
Labeler Code:
41520
Product Label ID:
084ed4fb-f95b-4d10-8678-10c3573fee97
Start Marketing Date: [9]
03-27-2018
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 41520-718-11

Package Description: 325 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 41520-718?

The NDC code 41520-718 is assigned by the FDA to the product Careone Medicated Dandruff With Menthol which is product labeled by American Sales Company. The product's dosage form is . The product is distributed in a single package with assigned NDC code 41520-718-11 325 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 Careone Medicated Dandruff With Menthol?

Shake well, wet hair, massage onto scalp and rinse.for best results, use at least twice a week or as directed by a doctor.

Which are Careone Medicated Dandruff With Menthol UNII Codes?

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

Which are Careone Medicated Dandruff With Menthol 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 Careone Medicated Dandruff With Menthol?

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:

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Patient Education

Selenium Sulfide


Selenium sulfide, an anti-infective agent, relieves itching and flaking of the scalp and removes the dry, scaly particles that are commonly referred to as dandruff or seborrhea. It is also used to treat tinea versicolor, a fungal infection of the skin. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
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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".