NDC 23710-052 Clease And Treat
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 23710-052?
What are the uses for Clease And Treat?
Which are Clease And Treat UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOYL PEROXIDE (UNII: W9WZN9A0GM)
- BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (Active Moiety)
- SELENIUM SULFIDE (UNII: Z69D9E381Q)
- SELENIUM (UNII: H6241UJ22B) (Active Moiety)
Which are Clease And Treat 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:
- AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
- CARBOMER 934 (UNII: Z135WT9208)
- GLYCERIN (UNII: PDC6A3C0OX)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- WATER (UNII: 059QF0KO0R)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- GLYCERYL RICINOLEATE (UNII: ZUE0CEL42O)
- TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)
What is the NDC to RxNorm Crosswalk for Clease And Treat?
- RxCUI: 797892 - salicylic acid 2 % Medicated Pad
- RxCUI: 797892 - salicylic acid 20 MG/ML Medicated Pad
- RxCUI: 797892 - salicylic acid 2 % Topical Swab
- RxCUI: 904807 - benzoyl peroxide 5 % Medicated Pad
- RxCUI: 904807 - benzoyl peroxide 50 MG/ML Medicated Pad
* 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".