NDC 98132-702 Bareminerals 5-in-1 Bb Advanced Performance Eyeshadow Broad Spectrum Spf 15 Soft Shell
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What is NDC 98132-702?
What are the uses for Bareminerals 5-in-1 Bb Advanced Performance Eyeshadow Broad Spectrum Spf 15 Soft Shell?
Which are Bareminerals 5-in-1 Bb Advanced Performance Eyeshadow Broad Spectrum Spf 15 Soft Shell 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 Bareminerals 5-in-1 Bb Advanced Performance Eyeshadow Broad Spectrum Spf 15 Soft Shell 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:
- ISODODECANE (UNII: A8289P68Y2)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- DIPALMITOYL HYDROXYPROLINE (UNII: E6AHA53N1H)
- MANGIFERA INDICA SEED BUTTER (UNII: 4OXD9M35X2)
- SAFFLOWER OIL (UNII: 65UEH262IS)
- CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60)
- DIACETYL BOLDINE (UNII: 37727Z7M0I)
- CALCIUM ALUMINUM BOROSILICATE (UNII: 3JRB8A35M0)
- STANNIC OXIDE (UNII: KM7N50LOS6)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- MICA (UNII: V8A1AW0880)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)
- CHROMIUM HYDROXIDE GREEN (UNII: RV8FT8XF5R)
- CHROMIC OXIDE (UNII: X5Z09SU859)
- FERRIC FERROCYANIDE (UNII: TLE294X33A)
- MANGANESE VIOLET (UNII: 72M48QQV8Q)
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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".