NDC 76144-223 Paulas Choice Defense Essential Glow Moisturizer Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 76144-223?
What are the uses for Paulas Choice Defense Essential Glow Moisturizer Spf 30?
Which are Paulas Choice Defense Essential Glow Moisturizer Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Paulas Choice Defense Essential Glow Moisturizer 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:
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- LEVOMENOL (UNII: 24WE03BX2T)
- LUTEIN (UNII: X72A60C9MT)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- WATER (UNII: 059QF0KO0R)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- SODIUM GLUCONATE (UNII: R6Q3791S76)
- XANTHAN GUM (UNII: TTV12P4NEE)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- ALUMINUM STEARATE (UNII: U6XF9NP8HM)
- LAURETH-7 (UNII: Z95S6G8201)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SOY STEROL (UNII: PL360EPO9J)
- ETHYL ACRYLATE/METHACRYLIC ACID/STEARETH-20 METHACRYLATE COPOLYMER (UNII: EPA1872R1N)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PULLULAN (UNII: 8ZQ0AYU1TT)
- BETASIZOFIRAN (UNII: 2X51AD1X3T)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV)
- GLYCERIN (UNII: PDC6A3C0OX)
- .ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01)
- ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- KIWI FRUIT (UNII: 71ES77LGJC)
- ARGAN OIL (UNII: 4V59G5UW9X)
- LINOLEIC ACID (UNII: 9KJL21T0QJ)
- RESVERATROL (UNII: Q369O8926L)
- ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)
- NIACINAMIDE (UNII: 25X51I8RD4)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
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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".