NDC 42248-130 Pro Laser Body
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42248 - Zenith Medicosm Sl
- 42248-130 - Pro Laser
Product Packages
NDC Code 42248-130-01
Package Description: 150 mL in 1 BOTTLE
Product Details
What is NDC 42248-130?
Which are Pro Laser Body UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Pro Laser Body 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:
- ALUMINUM OXIDE (UNII: LMI26O6933)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- COCONUT ACID (UNII: 40U37V505D)
- SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
- METHYLPARABEN SODIUM (UNII: CR6K9C2NHK)
- WATER (UNII: 059QF0KO0R)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- WHITE WAX (UNII: 7G1J5DA97F)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- GLYCERIN (UNII: PDC6A3C0OX)
- TROLAMINE (UNII: 9O3K93S3TK)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- HYDROLYZED ELASTIN, BOVINE, ALKALINE (1000 MW) (UNII: ZR28QKN0WT)
- CARBOMER 934 (UNII: Z135WT9208)
- IMIDUREA (UNII: M629807ATL)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- COLLAGEN, SOLUBLE, FISH SKIN (UNII: 8JC99XGU4W)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- ETHYLPARABEN (UNII: 14255EXE39)
- (2-CARBETHOXYETHYL)DIETHOXY(METHYL)SILANE (UNII: N28HAC3H5P)
- HYDROXYPROLINE (UNII: RMB44WO89X)
- ASPARTIC ACID (UNII: 30KYC7MIAI)
* 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".