NDC 58411-421 Cle De Peau Beaute Radiant Corrector For Eyes Ivory
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 58411-421?
What are the uses for Cle De Peau Beaute Radiant Corrector For Eyes Ivory?
Which are Cle De Peau Beaute Radiant Corrector For Eyes Ivory UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Cle De Peau Beaute Radiant Corrector For Eyes Ivory 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)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIISOSTEARYL MALATE (UNII: QBS8A3XZGQ)
- PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: TYP81E471F)
- PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
- SORBITAN SESQUIISOSTEARATE (UNII: VU97D01BF9)
- TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- TREHALOSE (UNII: B8WCK70T7I)
- CRATAEGUS MONOGYNA FLOWER (UNII: NT52AMP29J)
- SODIUM ACETYLATED HYALURONATE (UNII: WN66R7GL93)
- PEG/PPG-14/7 DIMETHYL ETHER (UNII: 6DNW9T7YT2)
- ROSA ROXBURGHII FRUIT (UNII: CVT1AA87FF)
- POLYQUATERNIUM-51 (2-METHACRYLOYLOXYETHYL PHOSPHORYLCHOLINE/N-BUTYL METHACRYLATE; 3:7) (UNII: EL9825H96J)
- CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- EDETATE TRISODIUM (UNII: 420IP921MB)
- SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- ALCOHOL (UNII: 3K9958V90M)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- TALC (UNII: 7SEV7J4R1U)
- SODIUM METABISULFITE (UNII: 4VON5FNS3C)
- HYDROGEN DIMETHICONE (13 CST) (UNII: 4QGR4P2YOI)
- STANNIC OXIDE (UNII: KM7N50LOS6)
- THEANINE (UNII: 8021PR16QO)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ETHYLPARABEN (UNII: 14255EXE39)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- MICA (UNII: V8A1AW0880)
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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".