NDC 10477-1003 All Physical Sunscreen Broad Spectrum Spf 50
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 10477-1003?
What are the uses for All Physical Sunscreen Broad Spectrum Spf 50?
Which are All Physical Sunscreen Broad Spectrum Spf 50 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 All Physical Sunscreen Broad Spectrum Spf 50 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)
- THERMUS THERMOPHILUS (UNII: 415H64SACF)
- POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
- SORBITOL (UNII: 506T60A25R)
- GLYCERIN (UNII: PDC6A3C0OX)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- WHITE WAX (UNII: 7G1J5DA97F)
- SQUALANE (UNII: GW89575KF9)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- PALMITOYL TRIPEPTIDE-5 (UNII: 2A3916MQHO)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- PALMITOYLLYSYLVALYLDIAMINOBUTYROYLTHREONINE (UNII: 1615WE9073)
- LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)
- YEAST, UNSPECIFIED (UNII: 3NY3SM6B8U)
- BORON NITRIDE (UNII: 2U4T60A6YD)
- EPIGALLOCATECHIN GALLATE (UNII: BQM438CTEL)
- UBIQUINONE Q2 (UNII: I7T5V2W47R)
- MELANIN SYNTHETIC (TYROSINE, PEROXIDE) (UNII: O0CV1RMR44)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- XANTHAN GUM (UNII: TTV12P4NEE)
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- SORBIC ACID (UNII: X045WJ989B)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- MAGNESIUM SULFATE HEPTAHYDRATE (UNII: SK47B8698T)
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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".