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  4. NDC Product Code: 73370-0001 R2b Wrinkle Cure Cream

NDC 73370-0001 R2b Wrinkle Cure Cream

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 73370-0001?
  4. R2b Wrinkle Cure Cream 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:
73370-0001
Proprietary Name:
R2b Wrinkle Cure Cream
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
R2b Korea Inc
Labeler Code:
73370
Product Label ID:
936f528e-9469-04ca-e053-2a95a90a442b
Start Marketing Date: [9]
09-26-2019
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 73370-0001-1

Package Description: 50 mL in 1 CONTAINER

NDC Code 73370-0001-2

Package Description: 25 mL in 1 TUBE

Product Details

What is NDC 73370-0001?

The NDC code 73370-0001 is assigned by the FDA to the product R2b Wrinkle Cure Cream which is product labeled by R2b Korea Inc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 73370-0001-1 50 ml in 1 container , 73370-0001-2 25 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 R2b Wrinkle Cure Cream?

Take an appropriate amount of this product and spread it evenly over your skin.

Which are R2b Wrinkle Cure Cream UNII Codes?

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

Which are R2b Wrinkle Cure Cream 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".