NDC 51769-901 Head And Shoulders Smooth And Silky
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 51769-901?
What are the uses for Head And Shoulders Smooth And Silky?
Which are Head And Shoulders Smooth And Silky 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 Smooth And Silky 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 LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- GLYCOL DISTEARATE (UNII: 13W7MDN21W)
- ZINC CARBONATE (UNII: EQR32Y7H0M)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- COCO MONOETHANOLAMIDE (UNII: C80684146D)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- MAGNESIUM CARBONATE HYDROXIDE (UNII: YQO029V1L4)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- POLYQUATERNIUM-10 (400 MPA.S AT 2%) (UNII: HB1401PQFS)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- MAGNESIUM SULFATE (UNII: DE08037SAB)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
What is the NDC to RxNorm Crosswalk for Head And Shoulders Smooth And Silky?
- RxCUI: 1043244 - head & shoulders 1 % Medicated Shampoo
- RxCUI: 1043244 - zinc pyrithione 10 MG/ML Medicated Shampoo [Head & Shoulders]
- RxCUI: 1043244 - Head & Shoulders 1 % Medicated Shampoo
- RxCUI: 1043244 - Head & Shoulders 10 MG/ML Medicated Shampoo
- RxCUI: 209884 - zinc pyrithione 1 % Medicated Shampoo
* 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".