NDC 69423-480 Head And Shoulders Grooming
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 69423-480?
What are the uses for Head And Shoulders Grooming?
Which are Head And Shoulders Grooming 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 Head And Shoulders Grooming 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:
- NIACINAMIDE (UNII: 25X51I8RD4)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- MINERAL OIL (UNII: T5L8T28FGP)
- DIOCTYL MALEATE (UNII: OD88G8439L)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- PANTHENOL (UNII: WV9CM0O67Z)
- CETEARETH-25 (UNII: 8FA93U5T67)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- POVIDONE K12 (UNII: 333AG72FWJ)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- PETROLATUM (UNII: 4T6H12BN9U)
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
- CARAMEL (UNII: T9D99G2B1R)
- CERESIN (UNII: Q1LS2UJO3A)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Head And Shoulders Grooming?
- RxCUI: 2104630 - Head & Shoulders 0.1 % Topical Cream
- RxCUI: 2104630 - zinc pyrithione 1 MG/ML Topical Cream [Head & Shoulders]
- RxCUI: 2104630 - Head & Shoulders 1 MG/ML Topical Cream
- RxCUI: 247812 - zinc pyrithione 0.1 % Topical Cream
- RxCUI: 247812 - zinc pyrithione 1 MG/ML Topical Cream
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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".