NDC 43538-290 Niseko Sunscreen Spf 25
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 43538-290?
Which are Niseko Sunscreen Spf 25 UNII Codes?
The UNII codes for the active ingredients in this product are:
- SULFACETAMIDE SODIUM (UNII: 4NRT660KJQ)
- SULFACETAMIDE (UNII: 4965G3J0F5) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Niseko Sunscreen Spf 25 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:
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DISODIUM OLEAMIDO MIPA-SULFOSUCCINATE (UNII: 0MBZ20845F)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- LEMON OIL (UNII: I9GRO824LL)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
- MAGNESIUM NITRATE (UNII: 77CBG3UN78)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- NIACINAMIDE (UNII: 25X51I8RD4)
- NONOXYNOL-20 (UNII: 60ZT1XYO5N)
- OCTOXYNOL-5 (UNII: TJ327E1R1V)
- WATER (UNII: 059QF0KO0R)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)
- SODIUM THIOSULFATE (UNII: HX1032V43M)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- XANTHAN GUM (UNII: TTV12P4NEE)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- ISODODECANE (UNII: A8289P68Y2)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)
- CETETH-10 PHOSPHATE (UNII: 4E05O5N49G)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- LAURETH-7 (UNII: Z95S6G8201)
* 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".