NDC 59078-125 Tonymoly My Sunny All In One Sun Spf45
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What is NDC 59078-125?
What are the uses for Tonymoly My Sunny All In One Sun Spf45?
Which are Tonymoly My Sunny All In One Sun Spf45 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Tonymoly My Sunny All In One Sun Spf45 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:
- PRUNUS MUME FRUIT (UNII: 639190I8CU)
- GELIDIUM CARTILAGINEUM (UNII: 37LBZ0E1UE)
- SQUALANE (UNII: GW89575KF9)
- PORTULACA OLERACEA WHOLE (UNII: D5J3623SV2)
- ENZACAMENE (UNII: 8I3XWY40L9)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- ORANGE (UNII: 5EVU04N5QU)
- OCTISALATE (UNII: 4X49Y0596W)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)
- ULVA COMPRESSA (UNII: SXZ209FM33)
- COCO GLUCOSIDE (UNII: ICS790225B)
- VANILLA (UNII: Q74T35078H)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- MACROCYSTIS PYRIFERA (UNII: K31S3OG5C4)
- ECKLONIA CAVA (UNII: UXX2N5V39P)
- LAMINARIA JAPONICA (UNII: WE98HW412B)
- NYMPHAEA ALBA FLOWER (UNII: 40KQ7Q535O)
- VISCUM ALBUM FRUIT (UNII: P83EQ521R3)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- TROMETHAMINE (UNII: 023C2WHX2V)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CHAMAECYPARIS OBTUSA LEAF (UNII: 7OL154J5XB)
- SANSEVIERIA TRIFASCIATA LEAF (UNII: S3B72UOI9O)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- DEHYDROACETIC ACID (UNII: 2KAG279R6R)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- ACETYL TETRAPEPTIDE-15 (UNII: 6K389LE0MV)
- WATER (UNII: 059QF0KO0R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- PEG-2 STEARATE (UNII: 94YQ11Y95F)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- GLYCOL STEARATE (UNII: 0324G66D0E)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- SODIUM PALMITOYL PROLINE (UNII: 64L053FRFO)
- CODIUM TOMENTOSUM (UNII: B8B45BRU87)
- SORBIC ACID (UNII: X045WJ989B)
- VISCUM ALBUM WHOLE (UNII: E6839Q6DO1)
- AVOBENZONE (UNII: G63QQF2NOX)
* Please review the disclaimer below.
[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".