NDC 42546-174 Sss Cleanser
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42546 - Prugen Pharmaceuticals
- 42546-174 - Sss Cleanser
Product Packages
NDC Code 42546-174-06
Package Description: 1 TUBE in 1 CARTON / 170.1 g in 1 TUBE
NDC Code 42546-174-16
Package Description: 1 BOTTLE in 1 CARTON / 453.6 g in 1 BOTTLE
Product Details
What is NDC 42546-174?
What are the uses for Sss Cleanser?
Which are Sss Cleanser UNII Codes?
The UNII codes for the active ingredients in this product are:
- SULFACETAMIDE SODIUM (UNII: 4NRT660KJQ)
- SULFACETAMIDE (UNII: 4965G3J0F5) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
Which are Sss Cleanser 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)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DISODIUM OLEAMIDO MONOETHANOLAMINE SULFOSUCCINATE (UNII: 5M1101WGSY)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- WATER (UNII: 059QF0KO0R)
- SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)
- SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)
- SODIUM THIOSULFATE (UNII: HX1032V43M)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- PETROLATUM (UNII: 4T6H12BN9U)
- XANTHAN GUM (UNII: TTV12P4NEE)
What is the NDC to RxNorm Crosswalk for Sss Cleanser?
- RxCUI: 999604 - sulfacetamide sodium 10 % / sulfur 1 % Medicated Liquid Soap
- RxCUI: 999604 - sulfacetamide sodium 100 MG/ML / sulfur 10 MG/ML Medicated Liquid Soap
* 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".