NDC 59279-507 Mediceuticals X-derma Dry Scalp And Hair Treatment
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What is NDC 59279-507?
What are the uses for Mediceuticals X-derma Dry Scalp And Hair Treatment?
Which are Mediceuticals X-derma Dry Scalp And Hair Treatment 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 Mediceuticals X-derma Dry Scalp And Hair Treatment 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- APIGENIN (UNII: 7V515PI7F6)
- BIOTIN (UNII: 6SO6U10H04)
- BIOTINOYL TRIPEPTIDE-1 (UNII: O6380721VA)
- 1-BUTENE (UNII: LY001N554L)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- CHAMOMILE (UNII: FGL3685T2X)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- COCO DIETHANOLAMIDE (UNII: 92005F972D)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- CUCUMBER SEED (UNII: BT3S9L53JK)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCERIN (UNII: PDC6A3C0OX)
- SUNFLOWER SEED (UNII: R9N3379M4Z)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- PANTHENOL (UNII: WV9CM0O67Z)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
- SIMMONDSIA CHINENSIS SEED WAX (UNII: 47X6Y9FJJ2)
- SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Mediceuticals X-derma Dry Scalp And Hair Treatment?
- RxCUI: 205173 - salicylic acid 1.8 % Medicated Shampoo
- RxCUI: 205173 - salicylic acid 18 MG/ML 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".