NDC 55789-1734 Anti-dandruff
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 55789-1734?
What are the uses for Anti-dandruff?
Which are Anti-dandruff UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Anti-dandruff 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)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- SODIUM LAUROYL HYDROXYPROPYL SULFONATE (UNII: IQ398K5X8M)
- COCO-BETAINE (UNII: 03DH2IZ3FY)
- SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- GLYCERIN (UNII: PDC6A3C0OX)
- PANTHENOL (UNII: WV9CM0O67Z)
- CUPRIC CARBONATE (UNII: 9AOA5F11GJ)
- ZINC CARBONATE (UNII: EQR32Y7H0M)
- MANGANESE CARBONATE (UNII: 9ZV57512ZM)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- UNDECYLENIC ACID (UNII: K3D86KJ24N)
- MICA (UNII: V8A1AW0880)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TEA TREE OIL (UNII: VIF565UC2G)
- GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
- OREGANO (UNII: 0E5AT8T16U)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
What is the NDC to RxNorm Crosswalk for Anti-dandruff?
- RxCUI: 205104 - salicylic acid 2 % Medicated Shampoo
- RxCUI: 205104 - salicylic acid 20 MG/ML Medicated Shampoo
- RxCUI: 205104 - salicylic acid 2 % 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".