NDC 42808-110 Sodium Sulfacetamide, Sulfur
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42808 - Exact-rx, Inc.
- 42808-110 - Sodium Sulfacetamide, Sulfur
Product Packages
NDC Code 42808-110-06
Package Description: 170 g in 1 TUBE
NDC Code 42808-110-12
Package Description: 2 TUBE in 1 CARTON / 170 g in 1 TUBE
Product Details
What is NDC 42808-110?
Which are Sodium Sulfacetamide, Sulfur 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 Sodium Sulfacetamide, Sulfur 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)
- DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
- SODIUM LAURYL SULFOACETATE (UNII: D0Y70F2B9J)
- SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)
- MINERAL OIL (UNII: T5L8T28FGP)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SODIUM THIOSULFATE (UNII: HX1032V43M)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- YELLOW WAX (UNII: 2ZA36H0S2V)
What is the NDC to RxNorm Crosswalk for Sodium Sulfacetamide, Sulfur?
- RxCUI: 999613 - sulfacetamide sodium 10 % / sulfur 5 % Medicated Liquid Soap
- RxCUI: 999613 - sulfacetamide sodium 100 MG/ML / sulfur 50 MG/ML Medicated Liquid Soap
- RxCUI: 999613 - sulfacetamide sodium 10 % / sulfur 5 % Topical Cleanser
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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".