NDC 58411-257 Shiseido Protective Lip Conditioner
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58411 - Shiseido Americas Corporation
- 58411-257 - Shiseido Protective Lip Conditioner
Product Packages
NDC Code 58411-257-20
Package Description: 1 CARTRIDGE in 1 CARTON / 4 g in 1 CARTRIDGE
Product Details
What is NDC 58411-257?
What are the uses for Shiseido Protective Lip Conditioner?
Which are Shiseido Protective Lip Conditioner UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Shiseido Protective Lip Conditioner 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:
- POLYGLYCERYL-2 TRIISOSTEARATE (UNII: 68DUY2D39A)
- TRIISOSTEARIN (UNII: 71503RH8KG)
- MACADAMIA OIL (UNII: 515610SU8C)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- DIPHENYLSILOXY PHENYL TRIMETHICONE (UNII: I445L28B12)
- TRIETHYLHEXANOIN (UNII: 7K3W1BIU6K)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- CANDELILLA WAX (UNII: WL0328HX19)
- MICA (UNII: V8A1AW0880)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- ARGININE HYDROCHLORIDE (UNII: F7LTH1E20Y)
- PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
- XYLITOL (UNII: VCQ006KQ1E)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- ALLANTOIN (UNII: 344S277G0Z)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- TRIMETHYLOLPROPANE TRIETHYLHEXANOATE (UNII: B952ZGW1IL)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- METHICONE (20 CST) (UNII: 6777U11MKT)
- TETRADECENE (UNII: FW23481S7S)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
* Please review the disclaimer below.
[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".