NDC 72934-8172 Salicylic Acid 5% / Sodium Sulfacetamide Monohydrate 10%
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72934 - Sincerus Florida, Llc
- 72934-8172 - Salicylic Acid 5% / Sodium Sulfacetamide Monohydrate 10%
Product Packages
NDC Code 72934-8172-6
Package Description: 120 g in 1 BOTTLE, PLASTIC
Product Details
What is NDC 72934-8172?
Which are Salicylic Acid 5% / Sodium Sulfacetamide Monohydrate 10% UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- SULFACETAMIDE SODIUM (UNII: 4NRT660KJQ)
- SULFACETAMIDE (UNII: 4965G3J0F5) (Active Moiety)
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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".