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NDC 37808-418 Dandruff 2 In 1 Shampoo And Conditioner Dry Scalp Recovery

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 37808-418?
  4. Dandruff 2 In 1 Shampoo And Conditioner Dry Scalp Recovery 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:
37808-418
Proprietary Name:
Dandruff 2 In 1 Shampoo And Conditioner Dry Scalp Recovery
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Heb
Labeler Code:
37808
Product Label ID:
db98bfa6-3f4b-499f-9b58-48020e511119
Start Marketing Date: [9]
10-20-2009
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 37808-418-14

Package Description: 420 mL in 1 BOTTLE, PLASTIC

NDC Code 37808-418-24

Package Description: 700 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 37808-418?

The NDC code 37808-418 is assigned by the FDA to the product Dandruff 2 In 1 Shampoo And Conditioner Dry Scalp Recovery which is product labeled by Heb. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 37808-418-14 420 ml in 1 bottle, plastic , 37808-418-24 700 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 2 In 1 Shampoo And Conditioner Dry Scalp Recovery?

HELPS PREVENT RECURRENCE OF FLAKING AND ITCHING ASSOCIATED WITH DANDRUFF

Which are Dandruff 2 In 1 Shampoo And Conditioner Dry Scalp Recovery UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Dandruff 2 In 1 Shampoo And Conditioner Dry Scalp Recovery?

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".