NDC 54111-136 Mario Badescu Collagen Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54111 - Bentley Laboratories Llc
- 54111-136 - Mario Badescu Collagen Spf 15
Product Packages
NDC Code 54111-136-50
Package Description: 59 mL in 1 BOTTLE, PLASTIC
NDC Code 54111-136-51
Package Description: 29 mL in 1 PACKAGE
Product Details
What is NDC 54111-136?
What are the uses for Mario Badescu Collagen Spf 15?
Which are Mario Badescu Collagen Spf 15 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)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Mario Badescu Collagen Spf 15 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:
- WATER (UNII: 059QF0KO0R)
- HYDROGENATED POLYBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ)
- COTTONSEED OIL (UNII: H3E878020N)
- ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- MARINE COLLAGEN, SOLUBLE (UNII: 8JC99XGU4W)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
* 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".