NDC 62742-4087 Daylight Tinted Radiance Moisturizer Broad Spectrum Spf 32 - Medium
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 62742-4087?
What are the uses for Daylight Tinted Radiance Moisturizer Broad Spectrum Spf 32 - Medium?
Which are Daylight Tinted Radiance Moisturizer Broad Spectrum Spf 32 - Medium UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Daylight Tinted Radiance Moisturizer Broad Spectrum Spf 32 - Medium 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)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- GLYCERIN (UNII: PDC6A3C0OX)
- MAGNOLIA OFFICINALIS BARK (UNII: 5M609NV974)
- ECTOINE (UNII: 7GXZ3858RY)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- TEPRENONE (UNII: S8S8451A4O)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- VITIS VINIFERA SEED (UNII: C34U15ICXA)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- ERGOTHIONEINE (UNII: BDZ3DQM98W)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TOCOPHEROL (UNII: R0ZB2556P8)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
- SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- MICA (UNII: V8A1AW0880)
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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".