NDC 82142-001 Legend Age Whitening Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 82142-001?
What are the uses for Legend Age Whitening Sunscreen?
Which are Legend Age Whitening Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Legend Age Whitening Sunscreen 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:
- POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
- HYDROGENATED POLYDECENE (1500 CST) (UNII: 4YI0729529)
- NIACINAMIDE (UNII: 25X51I8RD4)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- TOCOPHEROL (UNII: R0ZB2556P8)
- CAMELLIA JAPONICA SEED OIL (UNII: U37N0S910T)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- ALCOHOL (UNII: 3K9958V90M)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- XANTHAN GUM (UNII: TTV12P4NEE)
- MICA (UNII: V8A1AW0880)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- PENTAERYTHRITYL DISTEARATE (UNII: 697WOT8HNB)
- ENZACAMENE (UNII: 8I3XWY40L9)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- ETHYLHEXYL TRIAZONE (UNII: XQN8R9SAK4)
- TRICETEARETH-4 PHOSPHATE (UNII: 69534Y66NO)
- GLYCOL STEARATE (UNII: 0324G66D0E)
- DOCOSANOL (UNII: 9G1OE216XY)
- WATER (UNII: 059QF0KO0R)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PANTHENOL (UNII: WV9CM0O67Z)
- PEG-2 STEARATE (UNII: 94YQ11Y95F)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
- PEG-12 DIMETHICONE/PPG-20 CROSSPOLYMER (UNII: 965K72OQXO)
- ANGELICA GIGAS ROOT (UNII: 32766B2FHX)
- CNIDIUM OFFICINALE ROOT (UNII: 8S3OZD358J)
- PHENYLETHYL RESORCINOL (UNII: G37UFG162O)
- PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P)
- REHMANNIA GLUTINOSA ROOT (UNII: 1BEM3U6LQQ)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
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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".