NDC 58443-0195 Abella Colorshade Spf 35 Medium
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 58443-0195?
What are the uses for Abella Colorshade Spf 35 Medium?
Which are Abella Colorshade Spf 35 Medium UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Abella Colorshade Spf 35 Medium 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:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- ALMOND OIL (UNII: 66YXD4DKO9)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- BENTONITE (UNII: A3N5ZCN45C)
- CARAMEL (UNII: T9D99G2B1R)
- CETYL DIMETHICONE 45 (UNII: IK315POC44)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- ISOCETYL STEARATE (UNII: 3RJ7186O9W)
- MELANIN SYNTHETIC (TYROSINE, PEROXIDE) (UNII: O0CV1RMR44)
- WATER (UNII: 059QF0KO0R)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- OCTYL STEARATE (UNII: 772Y4UFC8B)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
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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".