NDC 56001-402 Bb Medium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 56001-402?
What are the uses for Bb Medium?
Which are Bb Medium UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Bb Medium 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)
- DIETHYLHEXYL CARBONATE (UNII: YCD50O0Z6L)
- CASTOR OIL (UNII: D5340Y2I9G)
- GLYCERIN (UNII: PDC6A3C0OX)
- ETHYL MACADAMIATE (UNII: ANA2NCS6V1)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- ISODODECANE (UNII: A8289P68Y2)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
- ABELMOSCHUS MOSCHATUS SEED (UNII: UN2QZ55I88)
- SQUALANE (UNII: GW89575KF9)
- PALMITOYL LYSYLDIOXYMETHIONYLLYSINE (UNII: T7A529FB8O)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- MAGNESIUM SULFATE (UNII: DE08037SAB)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- GLYCERYL DIBEHENATE (UNII: R8WTH25YS2)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- HYDROXYPROPYL .BETA.-CYCLODEXTRIN (UNII: 1I96OHX6EK)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- PHENYLETHYL RESORCINOL (UNII: G37UFG162O)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
* 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".