NDC 59735-308 Daily Fade Maximum Strength Spf15
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59735 - Biocosmetic Research Labs
- 59735-308 - Daily Fade
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?
What are the uses for Daily Fade Maximum Strength Spf15?
Which are Daily Fade Maximum Strength Spf15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROQUINONE (UNII: XV74C1N1AE)
- HYDROQUINONE (UNII: XV74C1N1AE) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
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[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".