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NDC 71006-090 Rubelli Beauty Face Premium

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71006-090?
  4. Rubelli Beauty Face Premium 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:
71006-090
Proprietary Name:
Rubelli Beauty Face Premium
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rubelli Co.,ltd
Labeler Code:
71006
Product Label ID:
07090918-7b2a-4c4d-9424-474a7a0544fb
Start Marketing Date: [9]
03-01-2019
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 71006-090?

The NDC code 71006-090 is assigned by the FDA to the product Rubelli Beauty Face Premium which is product labeled by Rubelli Co.,ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71006-090-02 7 pouch in 1 carton / 20 ml in 1 pouch (71006-090-01). 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 Rubelli Beauty Face Premium?

Directions:1. Please wash your face and make a sheet stick to your chin, neck, and cheeks to be the V shape.2. Please fix a pink band to your face as if you cover it and wear it to fit it.3. Please remove the mask sheet and the pink band after wearing them for about 30 to 60 minutes and dab parts with remaining essence so that it can be absorbed into skin.* You do not have to wash your face separately after using them.

Which are Rubelli Beauty Face Premium UNII Codes?

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

Which are Rubelli Beauty Face Premium 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:

* Please review the disclaimer below.

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".