NDC 44523-612 Sodium Sulfacetamide, Sulfur
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What is NDC 44523-612?
What are the uses for Sodium Sulfacetamide, Sulfur?
Which are Sodium Sulfacetamide, Sulfur UNII Codes?
The UNII codes for the active ingredients in this product are:
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
- SULFACETAMIDE SODIUM (UNII: 4NRT660KJQ)
- SULFACETAMIDE (UNII: 4965G3J0F5) (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:
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- WATER (UNII: 059QF0KO0R)
- SODIUM ALUMINIUM SILICATE (UNII: 058TS43PSM)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- LAPONITE (UNII: D703131383)
- SODIUM THIOSULFATE (UNII: HX1032V43M)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- XANTHAN GUM (UNII: TTV12P4NEE)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
What is the NDC to RxNorm Crosswalk for Sodium Sulfacetamide, Sulfur?
- RxCUI: 1000946 - sulfacetamide sodium 10 % / sulfur 4 % Medicated Pad
- RxCUI: 1000946 - sulfacetamide sodium 100 MG/ML / sulfur 40 MG/ML Medicated Pad
- RxCUI: 1000946 - sulfacetamide sodium 10 % / sulfur 4 % Topical Swab
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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".