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NDC 71673-0001 Dpc Aura Booster Mask

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71673-0001?
  4. Dpc Aura Booster Mask 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:
71673-0001
Proprietary Name:
Dpc Aura Booster Mask
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Msco
Labeler Code:
71673
Product Label ID:
56ff4b98-b527-39cb-e054-00144ff8d46c
Start Marketing Date: [9]
07-01-2017
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 71673-0001?

The NDC code 71673-0001 is assigned by the FDA to the product Dpc Aura Booster Mask which is product labeled by Msco. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71673-0001-1 5 pouch in 1 package / 25 g in 1 pouch. 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 Dpc Aura Booster Mask?

1. After cleansing wipe water and apply skin lotion on face. 2. Apply the mask evenly over the face for 10-20 minutes and remove. 3. Pad the left over residue lightly to absorb.

Which are Dpc Aura Booster Mask UNII Codes?

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

Which are Dpc Aura Booster Mask 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".