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  4. NDC Product Code: 43438-003 Iman Skin Tone Evener Bb Spf 15

NDC 43438-003 Iman Skin Tone Evener Bb Spf 15

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43438-003?
  4. Iman Skin Tone Evener Bb Spf 15 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:
43438-003
Proprietary Name:
Iman Skin Tone Evener Bb Spf 15
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Impala, Inc.
Labeler Code:
43438
Product Label ID:
8afbb956-f24d-42f8-b197-e8d341f8462c
Start Marketing Date: [9]
08-16-2012
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Code Structure Chart

Product Details

What is NDC 43438-003?

The NDC code 43438-003 is assigned by the FDA to the product Iman Skin Tone Evener Bb Spf 15 which is product labeled by Impala, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 43438-003-01 30 ml 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 Iman Skin Tone Evener Bb Spf 15?

Uses:Help prevent sunburn

Which are Iman Skin Tone Evener Bb Spf 15 UNII Codes?

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

Which are Iman Skin Tone Evener Bb Spf 15 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".