NDC 59158-759 Virtual Skin Super Natural Finish Spf 10
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 59158-759?
Which are Virtual Skin Super Natural Finish Spf 10 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Virtual Skin Super Natural Finish Spf 10 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)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- TALC (UNII: 7SEV7J4R1U)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- WHEAT BRAN (UNII: 6L966A1IMR)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- BLACK OLIVE (UNII: 2M6QWV94OC)
- POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
- PALMITIC ACID (UNII: 2V16EO95H1)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- LAURETH-7 (UNII: Z95S6G8201)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- LINOLEIC ACID (UNII: 9KJL21T0QJ)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- SORBIC ACID (UNII: X045WJ989B)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- 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".