NDC 64942-1235 Suave Nourishing Coconut And Shea Butter Antidandruff
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 64942-1235?
What are the uses for Suave Nourishing Coconut And Shea Butter Antidandruff?
Which are Suave Nourishing Coconut And Shea Butter Antidandruff UNII Codes?
The UNII codes for the active ingredients in this product are:
- PYRITHIONE ZINC (UNII: R953O2RHZ5)
- PYRITHIONE (UNII: 6GK82EC25D) (Active Moiety)
Which are Suave Nourishing Coconut And Shea Butter Antidandruff 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)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- TEA-DODECYLBENZENESULFONATE (UNII: 8HM7ZD48HN)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- PPG-9 (UNII: I29VQH0G0B)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
- COCONUT (UNII: 3RT3536DHY)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SHEA BUTTER (UNII: K49155WL9Y)
What is the NDC to RxNorm Crosswalk for Suave Nourishing Coconut And Shea Butter Antidandruff?
- 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".