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  4. NDC Product Code: 69133-020 Bioxidea Miracle 48 Excellence Gold Mask

NDC 69133-020 Bioxidea Miracle 48 Excellence Gold Mask

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69133-020?
  4. Bioxidea Miracle 48 Excellence Gold 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:
69133-020
Proprietary Name:
Bioxidea Miracle 48 Excellence Gold Mask
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cosmetics Institute Technology Co., Ltd.
Labeler Code:
69133
Product Label ID:
c145d06a-2ae9-42ef-8551-c05edee007ac
Start Marketing Date: [9]
07-01-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69133-020-01

Package Description: 3 GEL in 1 CARTON

Product Details

What is NDC 69133-020?

The NDC code 69133-020 is assigned by the FDA to the product Bioxidea Miracle 48 Excellence Gold Mask which is product labeled by Cosmetics Institute Technology Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69133-020-01 3 gel in 1 carton . 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 Bioxidea Miracle 48 Excellence Gold Mask?

Indications and Usage: After cleansing, place mask on your face. Leave it on for 20-30 minutes. Gently remove the mask and lightly massage any remaining serum into your skin. Do not rinse.

Which are Bioxidea Miracle 48 Excellence Gold Mask UNII Codes?

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

Which are Bioxidea Miracle 48 Excellence Gold 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".