NDC 72889-526 Bansbao Skin Brightening And Spots-removing
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72889 - Mengfei Li Inc.
- 72889-526 - Bansbao Skin Brightening And Spots-removing
Product Characteristics
Product Packages
NDC Code 72889-526-95
Package Description: 1 BOTTLE in 1 BOX / 50 g in 1 BOTTLE
Product Details
What is NDC 72889-526?
What are the uses for Bansbao Skin Brightening And Spots-removing?
Which are Bansbao Skin Brightening And Spots-removing UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Bansbao Skin Brightening And Spots-removing 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SQUALANE (UNII: GW89575KF9)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- HYDROXYETHYL UREA (UNII: MBQ7DDQ7AR)
- GLYCINE (UNII: TE7660XO1C)
- AMMONIUM POLYACRYLOYLDIMETHYL TAURATE (55000 MPA.S) (UNII: F01RIY4371)
- TOCOPHEROL (UNII: R0ZB2556P8)
- ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK)
- MANNOSE, L- (UNII: 2W3YE50TX8)
- POLYGALACTURONIC ACID (UNII: VV3XD4CL04)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- PRUNUS PERSICA FLOWER (UNII: 19GWB0JENH)
- NELUMBO NUCIFERA FLOWER (UNII: 61W322NLDV)
- HIBISCUS LAEVIS FLOWER (UNII: 10813RME15)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- FAGRAEA BERTEROANA FLOWER OIL (UNII: 6665W245VP)
* 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".