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NDC 72176-0200 Wrinkle Power Filling

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 72176-0200?
  4. Wrinkle Power Filling 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:
72176-0200
Proprietary Name:
Wrinkle Power Filling
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Gibest
Labeler Code:
72176
Product Label ID:
67e377b5-5159-4f14-e053-2991aa0a2e07
Start Marketing Date: [9]
03-01-2018
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 72176-0200?

The NDC code 72176-0200 is assigned by the FDA to the product Wrinkle Power Filling which is product labeled by Gibest. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72176-0200-1 5 ml in 1 tube . 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 Wrinkle Power Filling?

[How to Use]Towel dry after face washing.Apply thin layer to the direction of wrinkle. Keep patting gently for about 15 seconds.Try not to talk or move for at least 2 minutes until dry.Strain feeling of your skin will disappear naturally.Shake well before you use.The nature of Hydrolyzed Sponge, it may be pricking little bit depends on individual's skin condition. However, it is quite natural and proving for working to your skin.

Which are Wrinkle Power Filling UNII Codes?

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

Which are Wrinkle Power Filling 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".