NDC 51191-3016 Spf 25 Uva/uvb
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 51191-3016?
Which are Spf 25 Uva/uvb UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- ENSULIZOLE (UNII: 9YQ9DI1W42)
- ENSULIZOLE (UNII: 9YQ9DI1W42) (Active Moiety)
Which are Spf 25 Uva/uvb 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)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- GLYCERIN (UNII: PDC6A3C0OX)
- PEG-8/SMDI COPOLYMER (UNII: CCX72L6NY6)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-75 STEARATE (UNII: OT38R0N74H)
- PROPYLENE GLYCOL DICAPRYLATE/DICAPRATE (UNII: O4446S9CRA)
- TROMETHAMINE (UNII: 023C2WHX2V)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- COCO GLUCOSIDE (UNII: ICS790225B)
- .ALPHA.-BISABOLOL, (+/-)- (UNII: 36HQN158VC)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- XANTHAN GUM (UNII: TTV12P4NEE)
- EDETATE SODIUM (UNII: MP1J8420LU)
- COCONUT ALCOHOL (UNII: 13F4MW8Y9K)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- WHEAT GERM OIL (UNII: 14C97E680P)
- CORN OIL (UNII: 8470G57WFM)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CETETH-20 (UNII: I835H2IHHX)
- STEARETH-20 (UNII: L0Q8IK9E08)
- SUGARCANE (UNII: 81H2R5AOH3)
- ACER SACCHARUM SAP (UNII: 75UOH57984)
- BILBERRY (UNII: 9P2U39H18W)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- SOY PROTEIN (UNII: R44IWB3RN5)
- SOYBEAN OIL (UNII: 241ATL177A)
- MIMOSA TENUIFLORA BARK (UNII: 515MQE449I)
- ALMOND (UNII: 3Z252A2K9G)
- LEMON (UNII: 24RS0A988O)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- ROSMARINUS OFFICINALIS FLOWERING TOP OIL (UNII: OXN0D3N28L)
- CUPRESSUS SEMPERVIRENS LEAF OIL (UNII: M7QUY89S4O)
- THYME OIL (UNII: 2UK410MY6B)
- ORANGE (UNII: 5EVU04N5QU)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- BETASIZOFIRAN (UNII: 2X51AD1X3T)
- METHYLPROPANEDIOL (UNII: N8F53B3R4R)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- PELARGONIUM GRAVEOLENS FLOWER OIL (UNII: 3K0J1S7QGC)
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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".