NDC 59538-001 Biokera
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 59538-001?
What are the uses for Biokera?
Which are Biokera UNII Codes?
The UNII codes for the active ingredients in this product are:
- PYRITHIONE ZINC (UNII: R953O2RHZ5)
- PYRITHIONE ZINC (UNII: R953O2RHZ5) (Active Moiety)
Which are Biokera 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)
- SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- CHLOROPROPYLATE (UNII: GI03ROM7HQ)
- LINSEED OIL (UNII: 84XB4DV00W)
- HEXYL SALICYLATE (UNII: 8F78EY72YL)
- POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)
- LAURETH-4 (UNII: 6HQ855798J)
- GLYCOL DISTEARATE (UNII: 13W7MDN21W)
- COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- 3-IODO-1-PROPANOL (UNII: 2FR2742AOL)
- LACTIC ACID (UNII: 33X04XA5AT)
- ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
What is the NDC to RxNorm Crosswalk for Biokera?
- RxCUI: 209884 - zinc pyrithione 1 % Medicated Shampoo
- RxCUI: 209884 - zinc pyrithione 10 MG/ML Medicated Shampoo
- RxCUI: 209884 - zinc pyrithione 1 % Medicated Conditioner
* 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".