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  4. NDC Product Code: 41163-418 Equaline Dandruff Dry Scalp 2 In 1

NDC 41163-418 Equaline Dandruff Dry Scalp 2 In 1

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 41163-418?
  4. Equaline Dandruff Dry Scalp 2 In 1 Uses
  5. Active Ingredients UNII Codes
  6. 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:
41163-418
Proprietary Name:
Equaline Dandruff Dry Scalp 2 In 1
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Supervalu Inc
Labeler Code:
41163
Product Label ID:
20e034ee-9540-4488-8293-5bbea7c4d2c7
Start Marketing Date: [9]
07-01-2010
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 41163-418-14

Package Description: 420 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 41163-418?

The NDC code 41163-418 is assigned by the FDA to the product Equaline Dandruff Dry Scalp 2 In 1 which is product labeled by Supervalu Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 41163-418-14 420 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 Equaline Dandruff Dry Scalp 2 In 1?

FOR MAXIMUM DANDRUFF CONTROL, USE EVERY TIME YOU SHAMPOO. WET HAIR, MASSAGE ONTO SCALP AND RINSE. REPEAT IF DESIRE.

Which are Equaline Dandruff Dry Scalp 2 In 1 UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Equaline Dandruff Dry Scalp 2 In 1?

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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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".