NDC 59779-016 Pyrithione Zinc
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 59779-016?
What are the uses for Pyrithione Zinc?
Which are Pyrithione Zinc 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 Pyrithione Zinc 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)
- AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- POLYOXYL 100 STEARATE (UNII: YD01N1999R)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- CARBOMER 934 (UNII: Z135WT9208)
- SODIUM LAURETH-2 SULFATE (UNII: ZZQ59TY3KG)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- TRIMETHYL OCTADECYL AMMONIUM CHLORIDE (UNII: CZ70647U92)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
What is the NDC to RxNorm Crosswalk for Pyrithione Zinc?
- 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".