NDC 23637-001 Bioxsine Series
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 23637-001?
What are the uses for Bioxsine Series?
Which are Bioxsine Series 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 Bioxsine Series 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:
- APIGENIN (UNII: 7V515PI7F6)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK)
- CAROB (UNII: 5MG5Z946UO)
- CHAMOMILE (UNII: FGL3685T2X)
- EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z)
- URTICA DIOICA ROOT (UNII: J8HE8A6E5T)
- URTICA URENS LEAF (UNII: 0DCW2P163M)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- GERANIOL (UNII: L837108USY)
- GLYCERIN (UNII: PDC6A3C0OX)
- LAURETH-2 (UNII: D4D38LT1L5)
- POLIDOCANOL (UNII: 0AWH8BFG9A)
- HONEY (UNII: Y9H1V576FH)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- OLEANOLIC ACID (UNII: 6SMK8R7TGJ)
- PANTHENOL (UNII: WV9CM0O67Z)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- TRIDECETH-12 (UNII: YFY3KG5Y7O)
- VITIS VINIFERA SEED (UNII: C34U15ICXA)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Bioxsine Series?
- RxCUI: 426904 - zinc pyrithione 1.5 % Medicated Shampoo
- RxCUI: 426904 - zinc pyrithione 15 MG/ML Medicated Shampoo
* 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".