NDC 71460-001 Wiklar Uv Cover Shield
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 71460-001?
What are the uses for Wiklar Uv Cover Shield?
Which are Wiklar Uv Cover Shield UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Wiklar Uv Cover Shield 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)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- GLYCERIN (UNII: PDC6A3C0OX)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- BEMOTRIZINOL (UNII: PWZ1720CBH)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 3) (UNII: G300307ZXP)
- AMILOXATE (UNII: 376KTP06K8)
- NIACINAMIDE (UNII: 25X51I8RD4)
- GLYCERYL BEHENATE/EICOSADIOATE (UNII: 73CJJ317SR)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- NYLON-12 (UNII: 446U8J075B)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- CERESIN (UNII: Q1LS2UJO3A)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
- HYDROGEN DIMETHICONE (20 CST) (UNII: 12Z59IF64N)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
- ALUMINUM STEARATE (UNII: U6XF9NP8HM)
- TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- BOMBYX MORI FIBER (UNII: 6LK42KUV6W)
- PROPOLIS WAX (UNII: 6Y8XYV2NOF)
- ADENOSINE (UNII: K72T3FS567)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ETHOHEXADIOL (UNII: M9JGK7U88V)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
* 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".