NDC 31645-162 Mineral Wear Talc-free Mineral Airbrushing Blush Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 31645 - Physicians Formula Inc
- 31645-162 - Mineral Wear Talc-free Mineral Airbrushing Blush
Product Packages
NDC Code 31645-162-02
Package Description: 1 CONTAINER in 1 BOX / 3 g in 1 CONTAINER (31645-162-01)
Product Details
What is NDC 31645-162?
Which are Mineral Wear Talc-free Mineral Airbrushing Blush Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Mineral Wear Talc-free Mineral Airbrushing Blush 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:
- ZINC STEARATE (UNII: H92E6QA4FV)
- TRICAPRYLIN (UNII: 6P92858988)
- MAGNESIUM SILICATE (UNII: 9B9691B2N9)
- SAFFLOWER OIL (UNII: 65UEH262IS)
- CHAMOMILE (UNII: FGL3685T2X)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- GINKGO (UNII: 19FUJ2C58T)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
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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".