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  4. NDC Product Code: 49967-411 Vichy Laboratoires Normaderm Beautifying Anti Acne Care 24 H Hydrating Acne Treatment

NDC 49967-411 Vichy Laboratoires Normaderm Beautifying Anti Acne Care 24 H Hydrating Acne Treatment

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 49967-411?
  4. Vichy Laboratoires Normaderm Beautifying Anti Acne Care 24 H Hydrating Acne Treatment Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Get all the details for National Drug Code (NDC) 49967-411 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
49967-411
Proprietary Name:
Vichy Laboratoires Normaderm Beautifying Anti Acne Care 24 H Hydrating Acne Treatment
Product Type: [3]
Labeler Name: [5]
L'oreal Usa Products Inc
Labeler Code:
49967
Product Label ID:
f534314c-76bd-4ebf-a0f6-ab191c8ad55a
FDA Application Number: [6]
M006
Marketing Category: [8]
OTC MONOGRAPH DRUG -
Start Marketing Date: [9]
01-01-2016
End Marketing Date: [10]
08-18-2023
Listing Expiration Date: [11]
08-18-2023
Exclude Flag: [12]
D
Code Navigator:

Code Structure Chart

Product Details

What is NDC 49967-411?

The NDC code 49967-411 is assigned by the FDA to the product Vichy Laboratoires Normaderm Beautifying Anti Acne Care 24 H Hydrating Acne Treatment which is product labeled by L'oreal Usa Products Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 49967-411-01 1 bottle in 1 carton / 50 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 Vichy Laboratoires Normaderm Beautifying Anti Acne Care 24 H Hydrating Acne Treatment?

Cleanse the skin thoroughly before applying this productcover the entire affected area with a thin layer one to three times dailybecause too much drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctorif bothersome dryness or peeling occurs, reduce application to once a day or every other day

Which are Vichy Laboratoires Normaderm Beautifying Anti Acne Care 24 H Hydrating Acne Treatment UNII Codes?

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

Which are Vichy Laboratoires Normaderm Beautifying Anti Acne Care 24 H Hydrating Acne Treatment 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:

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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.

[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[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.

[10] What is the End Marketing Date? - This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

[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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".