NDC 81897-501 Rgo Daily Essence Sun
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 81897-501?
What are the uses for Rgo Daily Essence Sun?
Which are Rgo Daily Essence Sun UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Rgo Daily Essence Sun 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)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- LEVOMENOL (UNII: 24WE03BX2T)
- BUTETH-3 (UNII: OC116GRO69)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- LAURETH-23 (UNII: N72LMW566G)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- EUGENOL (UNII: 3T8H1794QW)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- JOJOBA OIL (UNII: 724GKU717M)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
- BEMOTRIZINOL (UNII: PWZ1720CBH)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- CETYL PALMITATE (UNII: 5ZA2S6B08X)
- SODIUM BENZOTRIAZOLYL BUTYLPHENOL SULFONATE (UNII: 0LA2QC9O3Z)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CYCLOMETHICONE 4 (UNII: CZ227117JE)
- LAURETH-4 (UNII: 6HQ855798J)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- TRIBUTYL CITRATE (UNII: 827D5B1B6S)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- DOCOSANOL (UNII: 9G1OE216XY)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- ALUMINUM STEARATE (UNII: U6XF9NP8HM)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- SQUALANE (UNII: GW89575KF9)
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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".