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  4. NDC Product Code: 71974-020 Skinmd Laboratories Pure Whitenol Intensive

NDC 71974-020 Skinmd Laboratories Pure Whitenol Intensive

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71974-020?
  4. Skinmd Laboratories Pure Whitenol Intensive 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 inactivated by the FDA.
NDC Product Code:
71974-020
Proprietary Name:
Skinmd Laboratories Pure Whitenol Intensive
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Reviresco Co., Ltd.
Labeler Code:
71974
Product Label ID:
7b9adc93-0d15-48d5-90f4-462d95643349
Start Marketing Date: [9]
12-01-2017
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 71974-020?

The NDC code 71974-020 is assigned by the FDA to the product Skinmd Laboratories Pure Whitenol Intensive which is product labeled by Reviresco Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71974-020-02 1 tube in 1 carton / 10 ml in 1 tube (71974-020-01). 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 Skinmd Laboratories Pure Whitenol Intensive?

Directions: Apply two times at morning and night onto the skin daily.

Which are Skinmd Laboratories Pure Whitenol Intensive UNII Codes?

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

Which are Skinmd Laboratories Pure Whitenol Intensive 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.

[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".