NDC 71516-002 Zinc Pyrithione
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 71516-002?
What are the uses for Zinc Pyrithione?
Which are Zinc Pyrithione 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 Zinc Pyrithione 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:
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- EQUISETUM ARVENSE BRANCH (UNII: 1L0VKZ185E)
- GLYCERIN (UNII: PDC6A3C0OX)
- GUAR GUM (UNII: E89I1637KE)
- HUMULUS LUPULUS STEM (UNII: OU3SJO07MD)
- AMINO ACIDS, SILK (UNII: V0L00EX1IA)
- BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61)
- PANTHENOL (UNII: WV9CM0O67Z)
- AMINO ACIDS, HAIR KERATIN (UNII: G46579QK1M)
- CORN (UNII: 0N8672707O)
- ARGANIA SPINOSA LEAF (UNII: 51XV5WTF7E)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SAW PALMETTO (UNII: J7WWH9M8QS)
- SIMMONDSIA CHINENSIS LEAF (UNII: 67G221EK95)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- SHEA BUTTER (UNII: K49155WL9Y)
- CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- COCONUT OIL (UNII: Q9L0O73W7L)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- WATER (UNII: 059QF0KO0R)
- CAMELLIA SINENSIS SEED OIL (UNII: O5R6DK2M9K)
What is the NDC to RxNorm Crosswalk for Zinc Pyrithione?
- RxCUI: 209884 - zinc pyrithione 1 % Medicated Shampoo
- RxCUI: 209884 - zinc pyrithione 10 MG/ML Medicated Shampoo
- RxCUI: 209884 - zinc pyrithione 1 % Medicated Conditioner
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[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".