NDC 80449-400 Sweat Mineral Foundation Spf 30 Shade 400
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 80449 - Sweat Cosmetics, Inc.
- 80449-400 - Sweat Mineral Foundation Spf 30
Product Packages
NDC Code 80449-400-01
Package Description: 1 CONTAINER in 1 BOX / 2.7 g in 1 CONTAINER
NDC Code 80449-400-02
Package Description: 1 CONTAINER in 1 BOX / 2.7 g in 1 CONTAINER
NDC Code 80449-400-03
Package Description: 1 JAR in 1 BOX / 12 g in 1 JAR
Product Details
What is NDC 80449-400?
What are the uses for Sweat Mineral Foundation Spf 30 Shade 400?
Which are Sweat Mineral Foundation Spf 30 Shade 400 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Sweat Mineral Foundation Spf 30 Shade 400 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:
- MICA (UNII: V8A1AW0880)
- BORON NITRIDE (UNII: 2U4T60A6YD)
- SQUALANE (UNII: GW89575KF9)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- TOCOPHEROL (UNII: R0ZB2556P8)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ISOPENTYLDIOL (UNII: 19NOL5474Q)
- MILK THISTLE (UNII: U946SH95EE)
- SEDUM ROSEUM ROOT (UNII: 3S5ITS5ULN)
- PROPANEDIOL (UNII: 5965N8W85T)
- WATER (UNII: 059QF0KO0R)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- 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".