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  4. NDC Product Code: 69712-010 Oroche Derma Rejuvenator

NDC 69712-010 Oroche Derma Rejuvenator

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69712-010?
  4. Oroche Derma Rejuvenator 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:
69712-010
Proprietary Name:
Oroche Derma Rejuvenator
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Oroche
Labeler Code:
69712
Product Label ID:
8ce7b1e4-7ca1-4af5-8c5c-79e565d459d9
Start Marketing Date: [9]
03-01-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 69712-010?

The NDC code 69712-010 is assigned by the FDA to the product Oroche Derma Rejuvenator which is product labeled by Oroche. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69712-010-01 12 ml in 1 carton . 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 Oroche Derma Rejuvenator?

Indications & Usage: Shake it up and down to mix the highly concentrated powder and activated liquid after turning the container upside down and twist it to the right - bust the inner membrance. Press the pump and take appropriate amount, then spread it onto the skin. After that pad the skin lightly for the product to be absorbed well. It is highly recommended to keep this mixed highly concentrated powder and ample in the refrigerator and to be consumed within 30 days.

Which are Oroche Derma Rejuvenator UNII Codes?

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

Which are Oroche Derma Rejuvenator 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".