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  4. NDC Product Code: 70484-006 Post Peel Protectant Vitality Institute

NDC 70484-006 Post Peel Protectant Vitality Institute

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70484-006?
  4. Post Peel Protectant Vitality Institute 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:
70484-006
Proprietary Name:
Post Peel Protectant Vitality Institute
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Vi Medical Products Inc.
Labeler Code:
70484
Product Label ID:
a62abbf3-546b-4edd-849b-3686a66e26b5
Start Marketing Date: [9]
03-25-2015
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 70484-006?

The NDC code 70484-006 is assigned by the FDA to the product Post Peel Protectant Vitality Institute which is product labeled by Vi Medical Products Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70484-006-02 1 tube in 1 box / 30 ml in 1 tube (70484-006-01). 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 Post Peel Protectant Vitality Institute?

Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 day or clear up and occur again within a few days, do not use this or any other hydrocortisone products unless you hav consulted a doctor.

Which are Post Peel Protectant Vitality Institute UNII Codes?

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

Which are Post Peel Protectant Vitality Institute 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".