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  4. NDC Product Code: 59735-306 Daily Fade Spf15

NDC 59735-306 Daily Fade Spf15

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 59735-306?
  4. Daily Fade Spf15 Uses
  5. Active 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:
59735-306
Proprietary Name:
Daily Fade Spf15
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Biocosetic Research Labs
Labeler Code:
59735
Product Label ID:
56056810-12a4-44de-a64d-dc134bced97a
Start Marketing Date: [9]
03-06-2006
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 59735-306?

The NDC code 59735-306 is assigned by the FDA to the product Daily Fade Spf15 which is product labeled by Biocosetic Research Labs. The product's dosage form is . The product is distributed in a single package with assigned NDC code 59735-306-56 1 tube in 1 carton / 56 g 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 Daily Fade Spf15?

UsesFor gradual fading of dark {brownish} spots.

Which are Daily Fade Spf15 UNII Codes?

The UNII codes for the active 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".