NDC 81521-001 Derm Institute Daily Defense Protection Sunscreen Broad Spectrum Spf50
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 81521-001?
What are the uses for Derm Institute Daily Defense Protection Sunscreen Broad Spectrum Spf50?
Which are Derm Institute Daily Defense Protection Sunscreen Broad Spectrum Spf50 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 Derm Institute Daily Defense Protection Sunscreen Broad Spectrum Spf50 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:
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- DIETHYLHEXYL CARBONATE (UNII: YCD50O0Z6L)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- CETYL ETHYLHEXANOATE (UNII: 134647WMX4)
- WATER (UNII: 059QF0KO0R)
- ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
- O-CYMEN-5-OL (UNII: H41B6Q1I9L)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- LUTEIN (UNII: X72A60C9MT)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- BACOPA MONNIERI WHOLE (UNII: DUB5K84ELI)
- SHEA BUTTER (UNII: K49155WL9Y)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ALLANTOIN (UNII: 344S277G0Z)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PROPANEDIOL (UNII: 5965N8W85T)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- POVIDONE (UNII: FZ989GH94E)
- ERGOTHIONEINE (UNII: BDZ3DQM98W)
- CHONDRUS CRISPUS CARRAGEENAN (UNII: UE856F2T78)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- POLYGLYCERYL-6 POLYRICINOLEATE (UNII: YPM0ZOC2HR)
- GLYCERIN (UNII: PDC6A3C0OX)
- PEG-12 GLYCERYL LAURATE (UNII: J07WW42G15)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5)
- MILK THISTLE (UNII: U946SH95EE)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- TOCOPHEROL (UNII: R0ZB2556P8)
- PROLINE (UNII: 9DLQ4CIU6V)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- TEA TREE OIL (UNII: VIF565UC2G)
- ADENOSINE TRIPHOSPHATE (UNII: 8L70Q75FXE)
- HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
- POLYOXYL 35 CASTOR OIL (UNII: 6D4M1DAL6O)
- XANTHAN GUM (UNII: TTV12P4NEE)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- ACETYL L-TYROSINE (UNII: DA8G610ZO5)
- UREA (UNII: 8W8T17847W)
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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".