NDC 54473-261 Sei Bella Tinted Bb Moisturizing Creme Broadspectrum Spf 20 Blush 140 C
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 54473-261?
What are the uses for Sei Bella Tinted Bb Moisturizing Creme Broadspectrum Spf 20 Blush 140 C?
Which are Sei Bella Tinted Bb Moisturizing Creme Broadspectrum Spf 20 Blush 140 C UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Sei Bella Tinted Bb Moisturizing Creme Broadspectrum Spf 20 Blush 140 C 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:
- LENTIL (UNII: 6O38V6B52O)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- WATER (UNII: 059QF0KO0R)
- ISODODECANE (UNII: A8289P68Y2)
- 1,1'-((1-METHYL-1,2-ETHANEDIYL)2-PROPENOIC ACID, BIS(OXY(1-METHYL-2,1-ETHANEDIYL))) ESTER (UNII: 2O70KL79K2)
- ISOAMYL LAURATE (UNII: M1SLX00M3M)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- MAGNESIUM SULFATE (UNII: DE08037SAB)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- STANNIC OXIDE (UNII: KM7N50LOS6)
- CITRULLUS LANATUS VAR. LANATUS WHOLE (UNII: 3J5I6254YO)
- GLYCERYL MONOUNDECYLENATE (UNII: IK8A76Q5G8)
- GLYCERIN (UNII: PDC6A3C0OX)
- OCTYLDODECYL OLEATE (UNII: MCA43PK7MH)
- ISOLAN (UNII: K7716TIH63)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- ISOAMYL COCOATE (UNII: 14OG46E98E)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- GLUCONOLACTONE (UNII: WQ29KQ9POT)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- MICA (UNII: V8A1AW0880)
- APPLE FRUIT OIL (UNII: 9NT987I3A8)
- LAMINARIA DIGITATA (UNII: 15E7C67EE8)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)
- CALCIUM GLUCONATE (UNII: SQE6VB453K)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
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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".