NDC 31645-173 Super Cc Plus Cream Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 31645-173?
Which are Super Cc Plus Cream Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Super Cc Plus Cream 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:
- WATER (UNII: 059QF0KO0R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CALCIUM ALUMINUM BOROSILICATE (UNII: 3JRB8A35M0)
- GLYCERIN (UNII: PDC6A3C0OX)
- TEPRENONE (UNII: S8S8451A4O)
- HYDROXYCAPRIC ACID (UNII: B41993WR8W)
- HYDROXYCAPRYLIC ACID (UNII: 0R6X0G0S8A)
- SHEA BUTTER (UNII: K49155WL9Y)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- LAURETH-12 (UNII: OAH19558U1)
- MICA (UNII: V8A1AW0880)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- XANTHAN GUM (UNII: TTV12P4NEE)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- 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".