NDC 52686-642 Shiseido Sun Protection Lip Treatment
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 52686 - Shiseido America Inc.
- 52686-642 - Shiseido Sun Protection Lip Treatment
Product Packages
NDC Code 52686-642-20
Package Description: 1 CARTRIDGE in 1 CARTON / 4 g in 1 CARTRIDGE
Product Details
What is NDC 52686-642?
What are the uses for Shiseido Sun Protection Lip Treatment?
Which are Shiseido Sun Protection Lip Treatment 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 Shiseido Sun Protection Lip Treatment 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)
- TRIISOSTEARIN (UNII: 71503RH8KG)
- HYDROGENATED POLYBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- PEG/PPG-36/41 DIMETHYL ETHER (UNII: GZ406N3R9F)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- STEARYL GLYCYRRHETINATE (UNII: 3YYE6VJS0P)
- GLUTATHIONE (UNII: GAN16C9B8O)
- ZINC MYRISTATE (UNII: K09A9E2GGO)
- THIOTAURINE (UNII: NQZ2D7AO62)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- DIISOSTEARYL MALATE (UNII: QBS8A3XZGQ)
- GLYCERIN (UNII: PDC6A3C0OX)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
* 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".