NDC 43596-0006 Lbel Supremacie Nx Jour Replenishing Daytime Face Spf 15 Normal To Oily Skin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43596 - Ventura Corporation, Ltd
- 43596-0006 - Lbel Supremacie Nx Jour Replenishing Daytime Face Spf 15 Normal To Oily Skin
Product Packages
NDC Code 43596-0006-0
Package Description: 1 mL in 1 POUCH
NDC Code 43596-0006-1
Package Description: 5 mL in 1 TUBE
NDC Code 43596-0006-2
Package Description: 50 mL in 1 JAR
Product Details
What is NDC 43596-0006?
What are the uses for Lbel Supremacie Nx Jour Replenishing Daytime Face Spf 15 Normal To Oily Skin?
Which are Lbel Supremacie Nx Jour Replenishing Daytime Face Spf 15 Normal To Oily Skin UNII Codes?
The UNII codes for the active ingredients in this product are:
- ENSULIZOLE (UNII: 9YQ9DI1W42)
- ENSULIZOLE (UNII: 9YQ9DI1W42) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Lbel Supremacie Nx Jour Replenishing Daytime Face Spf 15 Normal To Oily Skin 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)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- PEA (UNII: W4X7H8GYFM)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- TROLAMINE (UNII: 9O3K93S3TK)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PEG-75 STEARATE (UNII: OT38R0N74H)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ERYTHRITOL (UNII: RA96B954X6)
- SODIUM POLYSTYRENE SULFONATE (UNII: 1699G8679Z)
- XANTHAN GUM (UNII: TTV12P4NEE)
- TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828)
- CARBOMER INTERPOLYMER TYPE A (55000 MPA.S) (UNII: 59TL3WG5CO)
- CETETH-20 (UNII: I835H2IHHX)
- SORGHUM BICOLOR STEM JUICE (UNII: SKN30A294R)
- STEARETH-20 (UNII: L0Q8IK9E08)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- SORBIC ACID (UNII: X045WJ989B)
- EDETATE SODIUM (UNII: MP1J8420LU)
- ETHYLPARABEN (UNII: 14255EXE39)
- SQUALANE (UNII: GW89575KF9)
- CHLORELLA VULGARIS (UNII: RYQ4R60M02)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- BIOTINOYL TRIPEPTIDE-1 (UNII: O6380721VA)
- FD&C RED NO. 4 (UNII: X3W0AM1JLX)
* 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".