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  4. NDC Product Code: 43596-0190 Double Use Compact Spf 15 Gold Deluxe Edition Claire 4

NDC 43596-0190 Double Use Compact Spf 15 Gold Deluxe Edition Claire 4

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43596-0190?
  4. Double Use Compact Spf 15 Gold Deluxe Edition Claire 4 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:
43596-0190
Proprietary Name:
Double Use Compact Spf 15 Gold Deluxe Edition Claire 4
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Ventura Corporation Ltd
Labeler Code:
43596
Product Label ID:
b5e8afc2-2b5a-9a76-e053-2995a90a782e
Start Marketing Date: [9]
11-12-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 43596-0190-1

Package Description: 10 g in 1 BOTTLE

Product Details

What is NDC 43596-0190?

The NDC code 43596-0190 is assigned by the FDA to the product Double Use Compact Spf 15 Gold Deluxe Edition Claire 4 which is product labeled by Ventura Corporation Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 43596-0190-1 10 g in 1 bottle . 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 Double Use Compact Spf 15 Gold Deluxe Edition Claire 4?

Stop use and ask a doctor if rash occurs.

Which are Double Use Compact Spf 15 Gold Deluxe Edition Claire 4 UNII Codes?

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

Which are Double Use Compact Spf 15 Gold Deluxe Edition Claire 4 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".