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  4. NDC Product Code: 61543-0003 Sudden Change Derma Renewal Complex

NDC 61543-0003 Sudden Change Derma Renewal Complex

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 61543-0003?
  4. Sudden Change Derma Renewal Complex 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:
61543-0003
Proprietary Name:
Sudden Change Derma Renewal Complex
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cca Industries Inc.
Labeler Code:
61543
Product Label ID:
d49548e2-f883-4b31-8a96-3d58f9ce24b6
Start Marketing Date: [9]
04-01-2018
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 61543-0003?

The NDC code 61543-0003 is assigned by the FDA to the product Sudden Change Derma Renewal Complex which is product labeled by Cca Industries Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 61543-0003-0 1 tube in 1 box / 30 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 Sudden Change Derma Renewal Complex?

For sunsreen use: apply liberally 15 minutes before sun exposure. Use a water resistant sunscreen if swimming or sweating. Reapply at least every 2 hours. Children under 6 months: ask a doctor.

Which are Sudden Change Derma Renewal Complex UNII Codes?

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

Which are Sudden Change Derma Renewal Complex 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".