NDC 55655-271 Livests Moist Foundation 123
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55655 - Arsoa Honsha Corporation
- 55655-271 - Livests Moist Foundation 123
Product Packages
NDC Code 55655-271-81
Package Description: 1 BOTTLE, GLASS in 1 BOX / 20 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 55655-271?
What are the uses for Livests Moist Foundation 123?
Which are Livests Moist Foundation 123 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 Livests Moist Foundation 123 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)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- TALC (UNII: 7SEV7J4R1U)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- GLYCERIN (UNII: PDC6A3C0OX)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: TYP81E471F)
- CETYL ETHYLHEXANOATE (UNII: 134647WMX4)
- NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- MICA (UNII: V8A1AW0880)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- BETAINE (UNII: 3SCV180C9W)
- PHYTOSTERYL/ISOSTEARYL/CETYL/STEARYL/BEHENYL DIMER DILINOLEATE (UNII: 8N725H4EFN)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYGLYCERYL-2 TRIISOSTEARATE (UNII: 68DUY2D39A)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- TOCOPHEROL (UNII: R0ZB2556P8)
- HYDROGEN DIMETHICONE (20 CST) (UNII: 12Z59IF64N)
- HYDROXYPROLINE (UNII: RMB44WO89X)
- STEARYL GLYCYRRHETINATE (UNII: 3YYE6VJS0P)
- SQUALANE (UNII: GW89575KF9)
- TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
- PHYTOSTERYL/OCTYLDODECYL LAUROYL GLUTAMATE (UNII: 65954KGO9Q)
- PHYTOSTERYL MACADAMIATE (UNII: 233VSF903M)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- PALMITOYL PROLINE (UNII: I49727TDYF)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- SODIUM PALMITOYL SARCOSINATE (UNII: 7297LY09YF)
- MAGNESIUM PALMITOYL GLUTAMATE (UNII: DH37YM1F48)
- PALMITIC ACID (UNII: 2V16EO95H1)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- SAXIFRAGA STOLONIFERA LEAF (UNII: O3TMV4903H)
- CYNARA SCOLYMUS LEAF (UNII: B71UA545DE)
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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".