NDC 59779-316 Cvs Psoriasis Medicated
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 59779-316?
What are the uses for Cvs Psoriasis Medicated?
Which are Cvs Psoriasis Medicated 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 Cvs Psoriasis Medicated 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)
- AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
- GLYCERYL MONOOLEATE (UNII: 4PC054V79P)
- ZINC PIDOLATE (UNII: C32PQ86DH4)
- PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
- KUKUI NUT OIL (UNII: TP11QR7B8R)
- PANTHENOL (UNII: WV9CM0O67Z)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- RHUBARB (UNII: G280W4MW6E)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- SUNFLOWER SEED (UNII: R9N3379M4Z)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
What is the NDC to RxNorm Crosswalk for Cvs Psoriasis Medicated?
- RxCUI: 205023 - salicylic acid 3 % Medicated Shampoo
- RxCUI: 205023 - salicylic acid 30 MG/ML 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".