NDC 81716-002 Subir Eyelash

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
81716-002
Proprietary Name:
Subir Eyelash
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dream Polymer
Labeler Code:
81716
Start Marketing Date: [9]
03-30-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 81716-002-01

Package Description: .7 g in 1 POUCH

Product Details

What is NDC 81716-002?

The NDC code 81716-002 is assigned by the FDA to the product Subir Eyelash 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 81716-002-01 .7 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 Subir Eyelash?

• The perm cream needs to cover the full lash from root to tip for a good result.• Let the perm cream(step1) remain on the lashes for 12 ~ 20 minutes (depending on the texture of the lashes).• Clean the eyelid skin immediately after applying the cream to avoid irritation. Do not overuse the perm cream.• To determine if the perm process is complete, carefully lift one to two times lashes from the Rod with a applicator and check curl.

Which are Subir Eyelash UNII Codes?

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

  • ETHYL THIOGLYCOLATE (UNII: Z5SD8DD6CP)
  • ETHYL THIOGLYCOLATE (UNII: Z5SD8DD6CP) (Active Moiety)
  • .ALPHA.N-(METHOXYCARBONYL)-L-ARGININE (UNII: PE4EFA9P6E)
  • .ALPHA.N-(METHOXYCARBONYL)-L-ARGININE (UNII: PE4EFA9P6E) (Active Moiety)

Which are Subir Eyelash 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".