NDC 10967-686 Prevage Anti Aging Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 10967 - Revlon
- 10967-686 - Prevage Anti Aging Spf 30
Product Packages
NDC Code 10967-686-17
Package Description: 50 mL in 1 TUBE
Product Details
What is NDC 10967-686?
What are the uses for Prevage Anti Aging Spf 30?
Which are Prevage Anti Aging Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Prevage Anti Aging Spf 30 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:
- MICA (UNII: V8A1AW0880)
- DIMETHICONE 1000 (UNII: MCU2324216)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- CARBOMER 1342 (UNII: 809Y72KV36)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- HYDROXYDECYL UBIQUINOYL DIPALMITOYL GLYCERATE (UNII: OV1BT2N8RC)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- TREHALOSE (UNII: B8WCK70T7I)
- HYDROGENATED PALM GLYCERIDES (UNII: YCZ8EM144Q)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- POLYQUATERNIUM-51 (2-METHACRYLOYLOXYETHYL PHOSPHORYLCHOLINE/N-BUTYL METHACRYLATE; 4:1) (UNII: X8Q92E1CPM)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- FD&C RED NO. 4 (UNII: X3W0AM1JLX)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- 2-(4-(DIETHYLAMINO)-2-HYDROXYBENZOYL)BENZOIC ACID (UNII: X4K32L28QB)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- ACRYLIC ACID (UNII: J94PBK7X8S)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- SHEA BUTTER (UNII: K49155WL9Y)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- ERGOTHIONEINE (UNII: BDZ3DQM98W)
- UREA (UNII: 8W8T17847W)
- ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
* 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".