NDC 38755-0111 Oily Hair Dandruff Zerran International
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What is NDC 38755-0111?
What are the uses for Oily Hair Dandruff Zerran International?
Which are Oily Hair Dandruff Zerran International 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 Oily Hair Dandruff Zerran International 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:
- SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
- DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- CORYMBIA CITRIODORA LEAF OIL (UNII: M63U6N96EB)
- ARABICA COFFEE BEAN (UNII: 3SW678MX72)
- PANTHENOL (UNII: WV9CM0O67Z)
- MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
- ORANGE PEEL (UNII: TI9T76XD44)
- ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK)
- BITTER FENNEL (UNII: J5W36Y5WG8)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- GINKGO (UNII: 19FUJ2C58T)
- GLYCERIN (UNII: PDC6A3C0OX)
- SORBIC ACID (UNII: X045WJ989B)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
What is the NDC to RxNorm Crosswalk for Oily Hair Dandruff Zerran International?
- 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".