NDC 59279-516 X-folate Plus
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 59279-516?
What are the uses for X-folate Plus?
Which are X-folate Plus UNII Codes?
The UNII codes for the active ingredients in this product are:
- COAL TAR (UNII: R533ESO2EC)
- COAL TAR (UNII: R533ESO2EC) (Active Moiety)
Which are X-folate Plus 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:
- SULISOBENZONE (UNII: 1W6L629B4K)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- DICETYLDIMONIUM CHLORIDE (UNII: 6F4SX2007N)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
- MENTHOL (UNII: L7T10EIP3A)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- PANTHENOL (UNII: WV9CM0O67Z)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y)
- POLYQUATERNIUM-10 (1000 MPA.S AT 2%) (UNII: GMR4PEN8PK)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for X-folate Plus?
- RxCUI: 204681 - coal tar 5 % Medicated Shampoo
- RxCUI: 204681 - coal tar 50 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".