NDC 51769-140 Head And Shoulders Hair Loss Prevention
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 51769-140?
What are the uses for Head And Shoulders Hair Loss Prevention?
Which are Head And Shoulders Hair Loss Prevention 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 Hair Loss Prevention 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)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- COCO MONOETHANOLAMIDE (UNII: C80684146D)
- ZINC CARBONATE (UNII: EQR32Y7H0M)
- GLYCOL DISTEARATE (UNII: 13W7MDN21W)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
- MAGNESIUM SULFATE (UNII: DE08037SAB)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- MAGNESIUM CARBONATE HYDROXIDE (UNII: YQO029V1L4)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Head And Shoulders Hair Loss Prevention?
- 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
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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".