NDC 67938-2075 Pro Triple Protection Factor Broad Spectrum Spf 50 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 67938-2075?
What are the uses for Pro Triple Protection Factor Broad Spectrum Spf 50 Sunscreen?
Which are Pro Triple Protection Factor Broad Spectrum Spf 50 Sunscreen 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 OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Pro Triple Protection Factor Broad Spectrum Spf 50 Sunscreen 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)
- ISODODECANE (UNII: A8289P68Y2)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) (UNII: RLA2U05Z4Q)
- PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: TYP81E471F)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- RICINOLETH-40 (UNII: 6S0J4W9IQY)
- CARNOSINE (UNII: 8HO6PVN24W)
- DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- ACETYL FARNESYLCYSTEINE (UNII: KK6984C8O3)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- METHYL DIHYDROJASMONATE (SYNTHETIC) (UNII: 3GW44CIE3Y)
- ALLYL HEXANOATE (UNII: 3VH84A363D)
- ETHYL 2,4-DECADIENOATE, (2E,4Z)- (UNII: 79P6KS9Y5Z)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- 3-(3,4-METHYLENEDIOXYPHENYL)-2-METHYLPROPANAL (UNII: L65EG8H6PA)
- CHONDRUS CRISPUS CARRAGEENAN (UNII: UE856F2T78)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ARABIDOPSIS THALIANA (UNII: AI3L60HQ81)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- ERGOTHIONEINE (UNII: BDZ3DQM98W)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
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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".