NDC 59538-002 Biokera
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 59538-002?
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)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- LINSEED OIL (UNII: 84XB4DV00W)
- AMODIMETHICONE (800 CST) (UNII: 363Z2T48P7)
- POLYQUATERNIUM-11 (1000000 MW) (UNII: 0B44BS5IJS)
- HEXYL SALICYLATE (UNII: 8F78EY72YL)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- TRIDECETH-12 (UNII: YFY3KG5Y7O)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
What is the NDC to RxNorm Crosswalk for Biokera?
- RxCUI: 1043014 - zinc pyrithione 0.5 % Medicated Conditioner
- RxCUI: 1043014 - zinc pyrithione 5 MG/ML Medicated Shampoo
- RxCUI: 1043014 - zinc pyrithione 0.5 % Medicated Shampoo
- RxCUI: 1435365 - biokera 0.5 % Medicated Conditioner
- RxCUI: 1435365 - zinc pyrithione 5 MG/ML Medicated Shampoo [Biokera]
* 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".