NDC 69017-206 Matte Moisture Tint Sunscreen Broad Spectrum Spf 15 Porcelain
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 69017-206?
Which are Matte Moisture Tint Sunscreen Broad Spectrum Spf 15 Porcelain 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 CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Matte Moisture Tint Sunscreen Broad Spectrum Spf 15 Porcelain 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)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 4) (UNII: 8INO2K35FA)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- PHYTANTRIOL (UNII: 8LVI07A72W)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- NYLON-12 (UNII: 446U8J075B)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- TOCOPHEROL (UNII: R0ZB2556P8)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- ZINC CHLORIDE (UNII: 86Q357L16B)
- LYSINE (UNII: K3Z4F929H6)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ETHYLPARABEN (UNII: 14255EXE39)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- ISOPROPYLPARABEN (UNII: A6EOX47QK0)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- MICA (UNII: V8A1AW0880)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
* 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".