NDC 79596-097 Too Faced Bb Creme Complete Coverage Make-up Spf-20 Vanilla Glow
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What is NDC 79596-097?
What are the uses for Too Faced Bb Creme Complete Coverage Make-up Spf-20 Vanilla Glow?
Which are Too Faced Bb Creme Complete Coverage Make-up Spf-20 Vanilla Glow 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 Too Faced Bb Creme Complete Coverage Make-up Spf-20 Vanilla Glow 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:
- TRIETHYLHEXANOIN (UNII: 7K3W1BIU6K)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (UNII: 9E4CO0W6C5)
- ISOTRIDECYL ISONONANOATE (UNII: WEF51750MT)
- DECYL PALMITATE (UNII: SDD3SU9U0A)
- MICA (UNII: V8A1AW0880)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TOCOPHEROL (UNII: R0ZB2556P8)
- PIVALIC ACID (UNII: 813RE8BX41)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- WATER (UNII: 059QF0KO0R)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ROSA MULTIFLORA FRUIT (UNII: EZ5DSL4T27)
- AVERRHOA CARAMBOLA LEAF (UNII: HB7UP0QK1T)
- RHODOMYRTUS TOMENTOSA FRUIT (UNII: Q99511S58K)
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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".