NDC 75944-100 Sol Leon Sunscreen Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 75944-100?
What are the uses for Sol Leon Sunscreen Spf 15?
Which are Sol Leon Sunscreen Spf 15 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)
Which are Sol Leon Sunscreen Spf 15 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)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- HOMOSALATE (UNII: V06SV4M95S)
- AVOBENZONE (UNII: G63QQF2NOX)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- GLYCERIN (UNII: PDC6A3C0OX)
- STEARETH-21 (UNII: 53J3F32P58)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- STEARETH-2 (UNII: V56DFE46J5)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- OCTISALATE (UNII: 4X49Y0596W)
- SOYBEAN (UNII: L7HT8F1ZOD)
- POLYOXYL 100 STEARATE (UNII: YD01N1999R)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ETHYLPARABEN (UNII: 14255EXE39)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- LEVOMENOL (UNII: 24WE03BX2T)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- PANTHENOL (UNII: WV9CM0O67Z)
- EDETATE SODIUM (UNII: MP1J8420LU)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CARROT (UNII: L56Z1JK48B)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- JUGLANS REGIA LEAF (UNII: 85HKB87105)
- BETA CAROTENE (UNII: 01YAE03M7J)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
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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".