NDC 59279-502 Solv X
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 59279-502?
What are the uses for Solv X?
Which are Solv X 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 Solv X 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:
- ACETIC MONOETHANOLAMIDE (UNII: A9O0818TWD)
- AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- BIOTIN (UNII: 6SO6U10H04)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- COCO DIETHANOLAMIDE (UNII: 92005F972D)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- SARCOSINE (UNII: Z711V88R5F)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- INOSITOL (UNII: 4L6452S749)
- LINOLEIC ACID (UNII: 9KJL21T0QJ)
- LINOLENIC ACID (UNII: 0RBV727H71)
- MENTHOL (UNII: L7T10EIP3A)
- PANTHENOL (UNII: WV9CM0O67Z)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- ALCOHOL (UNII: 3K9958V90M)
- JOJOBA OIL (UNII: 724GKU717M)
- SORBITOL (UNII: 506T60A25R)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- WHEAT GERM OIL (UNII: 14C97E680P)
- WATER (UNII: 059QF0KO0R)
- ZINC SULFATE (UNII: 89DS0H96TB)
What is the NDC to RxNorm Crosswalk for Solv X?
- RxCUI: 1314479 - SOLV-X 1.8 % Medicated Shampoo
- RxCUI: 1314479 - salicylic acid 18 MG/ML Medicated Shampoo [Solv X]
- RxCUI: 1314479 - Solv X 18 MG/ML Medicated Shampoo
- RxCUI: 1314479 - Solv-X 1.8 % Medicated Shampoo
- RxCUI: 205173 - salicylic acid 1.8 % 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".