NDC 62499-445 Spf 15 Anti-shine Moisturizing
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 62499-445?
What are the uses for Spf 15 Anti-shine Moisturizing?
Which are Spf 15 Anti-shine Moisturizing UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Spf 15 Anti-shine Moisturizing 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)
- BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)
- GLYCERIN (UNII: PDC6A3C0OX)
- METHYL GLUCETH-20 (UNII: J3QD0LD11P)
- GRAPE SEED OIL (UNII: 930MLC8XGG)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- METHYL METHACRYLATE (UNII: 196OC77688)
- SACCHARIDE ISOMERATE (UNII: W8K377W98I)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- .ALPHA.-GLUCAN OLIGOSACCHARIDE (UNII: S95658MI3W)
- TALC (UNII: 7SEV7J4R1U)
- SODIUM PALMITOYL PROLINE (UNII: 64L053FRFO)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLUCAMINE (UNII: 5QN16UUF80)
- OLEA EUROPAEA LEAF (UNII: MJ95C3OH47)
- NYMPHAEA ALBA FLOWER (UNII: 40KQ7Q535O)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- POVIDONE K30 (UNII: U725QWY32X)
- LESSER GALANGAL ROOT (UNII: 42LD90786Y)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- SARCOSINE (UNII: Z711V88R5F)
- CLARY SAGE OIL (UNII: 87L0D4U3M0)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- ORANGE OIL (UNII: AKN3KSD11B)
- MANDARIN OIL (UNII: NJO720F72R)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- LEMON OIL (UNII: I9GRO824LL)
- LIME OIL (UNII: UZH29XGA8G)
- WEST INDIAN LEMONGRASS OIL (UNII: 5BIA40E9ED)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- XANTHAN GUM (UNII: TTV12P4NEE)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
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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".