NDC 62742-4170 Prevention Plus Daily Tinted Moisturizer Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 62742-4170?
What are the uses for Prevention Plus Daily Tinted Moisturizer Spf 30?
Which are Prevention Plus Daily Tinted 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)
Which are Prevention Plus Daily Tinted 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:
- WATER (UNII: 059QF0KO0R)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCERYL STEARATE CITRATE (UNII: WH8T92A065)
- PEG-100 STEARATE (UNII: YD01N1999R)
- SHEA BUTTER (UNII: K49155WL9Y)
- STYRENE/ACRYLAMIDE COPOLYMER (500000 MW) (UNII: 5Z4DPO246A)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- ISOSTEARIC ACID (UNII: X33R8U0062)
- POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- POLYSILICONE-15 (UNII: F8DRP5BB29)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
- STEARETH-20 METHACRYLATE (UNII: A268NZ57NB)
- CITRUS AURANTIUM FRUIT OIL (UNII: 59JDQ5VT0T)
- HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ALLANTOIN (UNII: 344S277G0Z)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- LAMINARIA DIGITATA (UNII: 15E7C67EE8)
- ARTEMISIA VULGARIS TOP OIL (UNII: 72Q967Y48V)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- MANDARIN OIL (UNII: NJO720F72R)
- XANTHAN GUM (UNII: TTV12P4NEE)
- LEVOMENOL (UNII: 24WE03BX2T)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- ERYTHRITOL (UNII: RA96B954X6)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)
- VANILLA (UNII: Q74T35078H)
- ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK)
- PEA PROTEIN (UNII: 7Q50F46595)
- PYRUVIC ACID (UNII: 8558G7RUTR)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- AGATHOSMA BETULINA LEAF OIL (UNII: KOS935A04V)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- MAGNESIUM OXIDE (UNII: 3A3U0GI71G)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- HOMARINE HYDROCHLORIDE (UNII: 8866LNG61N)
- SODIUM SUCCINATE ANHYDROUS (UNII: V8ZGC8ISR3)
- ARABIDOPSIS THALIANA (UNII: AI3L60HQ81)
- MICROCOCCUS LUTEUS (UNII: LV6L29Z6AX)
- ANACYSTIS NIDULANS (UNII: UV4FTL6UAW)
- ERGOTHIONEINE (UNII: BDZ3DQM98W)
* 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".