NDC 59735-308 Daily Fade Maximum Strength Spf15

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
59735-308
Proprietary Name:
Daily Fade Maximum Strength Spf15
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Biocosmetic Research Labs
Labeler Code:
59735
Start Marketing Date: [9]
06-03-2009
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 59735-308-56

Package Description: 1 TUBE in 1 CARTON / 56.8 g in 1 TUBE

Product Details

What is NDC 59735-308?

The NDC code 59735-308 is assigned by the FDA to the product Daily Fade Maximum Strength Spf15 which is product labeled by Biocosmetic Research Labs. The product's dosage form is . The product is distributed in a single package with assigned NDC code 59735-308-56 1 tube in 1 carton / 56.8 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 Maximum Strength Spf15?

Uses:For gradual fading of dark (brownish) spots.  This product is not intended for use in the prevention of sunburn.

Which are Daily Fade Maximum Strength Spf15 UNII Codes?

The UNII codes for the active 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".