NDC 71305-200 Studio Blend Cover Foundation Spf15
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 71305-200?
What are the uses for Studio Blend Cover Foundation Spf15?
Which are Studio Blend Cover Foundation Spf15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Studio Blend Cover Foundation Spf15 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)
- ISODODECANE (UNII: A8289P68Y2)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- GLYCERIN (UNII: PDC6A3C0OX)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT)
- PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- METHICONE (20 CST) (UNII: 6777U11MKT)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- 4-HYDROXY ACETOPHENONE (UNII: G1L3HT4CMH)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
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[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".