NDC 59189-101 Radiance Cc Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 59189-101?
What are the uses for Radiance Cc Spf 30?
Which are Radiance Cc Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Radiance Cc Spf 30 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:
- ALOE VERA WHOLE (UNII: KIZ4X2EHYX)
- RUBUS URSINUS WHOLE (UNII: EB3AN7DKSL)
- KIWI FRUIT (UNII: 71ES77LGJC)
- POMEGRANATE JUICE (UNII: 99S671U9KB)
- GRAPE (UNII: 6X543N684K)
- JOJOBA OIL (UNII: 724GKU717M)
- ARGAN OIL (UNII: 4V59G5UW9X)
- BORAGE OIL (UNII: F8XAG1755S)
- CRANBERRY SEED OIL (UNII: 73KDS3BW5E)
- ROSA CANINA FRUIT OIL (UNII: CR7307M3QZ)
- RUBUS IDAEUS SEED (UNII: M3CL7US2ZG)
- SAFFLOWER OIL (UNII: 65UEH262IS)
- COCONUT OIL (UNII: Q9L0O73W7L)
- GLYCERIN (UNII: PDC6A3C0OX)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERROUS OXIDE (UNII: G7036X8B5H)
- STARCH, TAPIOCA (UNII: 24SC3U704I)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- GLYCERYL 1-UNDECYLENATE (UNII: B68LJT9544)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- LINALOOL, (+)- (UNII: F4VNO44C09)
* 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".