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NDC 81716-006 Subir

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 81716-006?
  4. Subir 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:
81716-006
Proprietary Name:
Subir
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dream Polymer
Labeler Code:
81716
Product Label ID:
ad369701-277a-41f4-a84c-5aee0ad64ac9
Start Marketing Date: [9]
03-30-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 81716-006?

The NDC code 81716-006 is assigned by the FDA to the product Subir which is product labeled by Dream Polymer. The product's dosage form is . The product is distributed in a single package with assigned NDC code 81716-006-01 10 g in 1 container . 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 Subir?

 After washing face, apply an appropriate amount of content to the brush. Apply to the root area of the eyelashes using the tip. Apply to eyelashes using a mascara brush. May also be used on eyebrows. It is recommended to use it twice a day in the morning and evening.

Which are Subir UNII Codes?

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

Which are Subir 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".