NDC 52554-3001 Laser Block 100 Sunblock
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 52554 - Universal Cosmetic Co., Ltd
- 52554-3001 - Laser Block 100
Product Packages
NDC Code 52554-3001-1
Package Description: 50 mL in 1 TUBE
Product Details
What is NDC 52554-3001?
Which are Laser Block 100 Sunblock UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- ENZACAMENE (UNII: 8I3XWY40L9)
- ENZACAMENE (UNII: 8I3XWY40L9) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- AMILOXATE (UNII: 376KTP06K8)
- AMILOXATE (UNII: 376KTP06K8) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (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".