NDC 65966-111 The Treatment Powder Foundation Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 65966 - Max Huber Research Lab Inc
- 65966-111 - The Treatment Powder Foundation
Product Packages
NDC Code 65966-111-01
Package Description: 1 JAR in 1 CARTON / 10 g in 1 JAR (65966-111-02)
Product Details
What is NDC 65966-111?
Which are The Treatment Powder Foundation 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)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are The Treatment Powder Foundation 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:
- TALC (UNII: 7SEV7J4R1U)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- BORON NITRIDE (UNII: 2U4T60A6YD)
- OCTYLDODECYL STEAROYL STEARATE (UNII: 3D47Q6D93C)
- YEAST (UNII: 3NY3SM6B8U)
- CUPRIC CARBONATE (UNII: 9AOA5F11GJ)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- GAMMA ORYZANOL (UNII: SST9XCL51M)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SORBIC ACID (UNII: X045WJ989B)
- BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- 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".