1. Home
  2. Labeler Index
  3. Ybk Investment, Inc
  4. NDC Product Code: 60709-107 Nano Ppc

NDC 60709-107 Nano Ppc

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 60709-107?
  4. Nano Ppc 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:
60709-107
Proprietary Name:
Nano Ppc
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Ybk Investment, Inc
Labeler Code:
60709
Product Label ID:
96e4d5fe-f459-41f7-b446-342c12880223
Start Marketing Date: [9]
11-15-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 60709-107?

The NDC code 60709-107 is assigned by the FDA to the product Nano Ppc which is product labeled by Ybk Investment, Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 60709-107-02 1 tube in 1 carton / 250 ml in 1 tube (60709-107-01). 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 Nano Ppc?

Direction for useApply suitable amount of the cream on target area.Gently massage for 3 minutes until it is absorbed. Cleanse with tissue or water.

Which are Nano Ppc UNII Codes?

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

Which are Nano Ppc 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".