NDC 65966-010 The Radiant Concealer Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 65966 - Max Huber Research Lab Inc
- 65966-010 - The Radiant Concealer
Product Packages
NDC Code 65966-010-01
Package Description: 1 JAR in 1 CARTON / 3.5 g in 1 JAR (65966-010-02)
Product Details
What is NDC 65966-010?
Which are The Radiant Concealer Spf 15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are The Radiant Concealer Spf 15 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:
- METHYL METHACRYLATE (UNII: 196OC77688)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- CANDELILLA WAX (UNII: WL0328HX19)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ROSEMARY (UNII: IJ67X351P9)
- SOYBEAN OIL (UNII: 241ATL177A)
- SEAWEED (UNII: 477TV3P5UX)
- FU LING (UNII: XH37TWY5O4)
- MAGNESIUM SILICATE (UNII: 9B9691B2N9)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- CUPRIC CARBONATE (UNII: 9AOA5F11GJ)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- LEVOMENOL (UNII: 24WE03BX2T)
- PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
- HYDROGENATED COTTONSEED OIL (UNII: Z82Y2C65EA)
- STANNIC OXIDE (UNII: KM7N50LOS6)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- MICA (UNII: V8A1AW0880)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
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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".