NDC 51523-111 Face It Oil Cut Dual Bb Emulsion Spf20
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 51523-111?
What are the uses for Face It Oil Cut Dual Bb Emulsion Spf20?
Which are Face It Oil Cut Dual Bb Emulsion Spf20 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 Face It Oil Cut Dual Bb Emulsion Spf20 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:
- WATER (UNII: 059QF0KO0R)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- TALC (UNII: 7SEV7J4R1U)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
- BETULA PLATYPHYLLA VAR. JAPONICA BARK (UNII: ZF70YKN0YO)
- RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C)
- CITRAL (UNII: T7EU0O9VPP)
- HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- MUNG BEAN (UNII: 1LIB31N73G)
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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".