NDC 76485-1055 Match Perfection Foundation Spf 20 - Shade 201 Classic Beige
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 76485-1055?
What are the uses for Match Perfection Foundation Spf 20 - Shade 201 Classic Beige?
Which are Match Perfection Foundation Spf 20 - Shade 201 Classic Beige 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)
Which are Match Perfection Foundation Spf 20 - Shade 201 Classic Beige 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)
- TALC (UNII: 7SEV7J4R1U)
- DICAPRYLYL ETHER (UNII: 77JZM5516Z)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 3) (UNII: G300307ZXP)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
- QUATERNIUM-91 (UNII: 00J8H295NB)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- MICA (UNII: V8A1AW0880)
- TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- MONTMORILLONITE (UNII: A585MN1H2L)
- AMMONIA (UNII: 5138Q19F1X)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)
- ALCOHOL (UNII: 3K9958V90M)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- DECETH-6 (UNII: P4OYN7A2O9)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- LAURETH-4 (UNII: 6HQ855798J)
- LAURETH-30 (UNII: W9D845551A)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
* 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".