NDC 75944-200 Sol Leon Sunscreen Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 75944-200?
What are the uses for Sol Leon Sunscreen Spf 30?
Which are Sol Leon Sunscreen Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Sol Leon Sunscreen Spf 30 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)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- HOMOSALATE (UNII: V06SV4M95S)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- GLYCERIN (UNII: PDC6A3C0OX)
- COCO-GLYCERIDES (UNII: ISE9I7DNUG)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- OCTISALATE (UNII: 4X49Y0596W)
- AVOBENZONE (UNII: G63QQF2NOX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- STEARETH-21 (UNII: 53J3F32P58)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- STEARETH-2 (UNII: V56DFE46J5)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYOXYL 100 STEARATE (UNII: YD01N1999R)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CARROT (UNII: L56Z1JK48B)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- DICHLOROBENZYL ALCOHOL (UNII: 1NKX3648J9)
- ETHYLPARABEN (UNII: 14255EXE39)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- LEVOMENOL (UNII: 24WE03BX2T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- PANTHENOL (UNII: WV9CM0O67Z)
- EDETATE SODIUM (UNII: MP1J8420LU)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- JUGLANS REGIA LEAF (UNII: 85HKB87105)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
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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".