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  4. NDC Product Code: 82439-102 Bff Skin Perfector Spf 30 Broad Spectrum Sunscreen Light

NDC 82439-102 Bff Skin Perfector Spf 30 Broad Spectrum Sunscreen Light

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 82439-102?
  4. Bff Skin Perfector Spf 30 Broad Spectrum Sunscreen Light 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:
82439-102
Proprietary Name:
Bff Skin Perfector Spf 30 Broad Spectrum Sunscreen Light
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Trinny London Ltd
Labeler Code:
82439
Product Label ID:
da35c5ee-bd9b-018f-e053-2a95a90a4655
Start Marketing Date: [9]
01-14-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

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Product Details

What is NDC 82439-102?

The NDC code 82439-102 is assigned by the FDA to the product Bff Skin Perfector Spf 30 Broad Spectrum Sunscreen Light which is product labeled by Trinny London Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 82439-102-01 30 ml in 1 box . 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 Bff Skin Perfector Spf 30 Broad Spectrum Sunscreen Light?

Stop use and ask a doctorif rash occurs

Which are Bff Skin Perfector Spf 30 Broad Spectrum Sunscreen Light UNII Codes?

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

Which are Bff Skin Perfector Spf 30 Broad Spectrum Sunscreen Light 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:

* Please review the disclaimer below.

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".