NDC 43596-0881 Studio Look Base De Alta Cobertura Para El Rostro Con Fps 20 Chocotrufa 430-n
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43596 - Ventura Corporation Ltd
- 43596-0881 - Studio Look Base De Alta Cobertura Para El Rostro Con Fps 20 Chocotrufa 430-n
Product Packages
NDC Code 43596-0881-1
Package Description: 30 g in 1 TUBE
Product Details
What is NDC 43596-0881?
What are the uses for Studio Look Base De Alta Cobertura Para El Rostro Con Fps 20 Chocotrufa 430-n?
Which are Studio Look Base De Alta Cobertura Para El Rostro Con Fps 20 Chocotrufa 430-n 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)
Which are Studio Look Base De Alta Cobertura Para El Rostro Con Fps 20 Chocotrufa 430-n 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:
- CHLORPHENESIN (UNII: I670DAL4SZ)
- PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- HELIANTHUS ANNUUS SEED WAX (UNII: 42DG15CHXV)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ISODODECANE (UNII: A8289P68Y2)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- POLYGLYCERIN-3 (UNII: 4A0NCJ6RD6)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYMETHYLSILSESQUIOXANE (11 MICRONS) (UNII: Z570VEV8XK)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
- TRIMETHYLSILOXYSILICATE (M/Q 1.0-1.2) (UNII: 78GX033D7I)
- ACACIA DECURRENS FLOWER WAX (UNII: AU6XZE9IY9)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
- WATER (UNII: 059QF0KO0R)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- LAURETH-12 (UNII: OAH19558U1)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
* 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".