NDC 57913-2815 Luminous Intensive Decollote Treatment Spf 20
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57913 - Erno Laszlo, Inc.
- 57913-2815 - Luminous Intensive Decollote Treatment Spf 20
Product Packages
NDC Code 57913-2815-0
Package Description: 1 JAR in 1 CARTON / 50 mL in 1 JAR
Product Details
What is NDC 57913-2815?
What are the uses for Luminous Intensive Decollote Treatment Spf 20?
Which are Luminous Intensive Decollote Treatment Spf 20 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Luminous Intensive Decollote Treatment Spf 20 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:
- CYCLOMETHICONE (UNII: NMQ347994Z)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- ISOPROPYLPARABEN (UNII: A6EOX47QK0)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
* Please review the disclaimer below.
[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".