NDC 21695-188 Mupirocin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21695 - Rebel Distributors Corp.
- 21695-188 - Mupirocin
Product Packages
NDC Code 21695-188-22
Package Description: 22 g in 1 TUBE
Product Details
What is NDC 21695-188?
What are the uses for Mupirocin?
Which are Mupirocin UNII Codes?
The UNII codes for the active ingredients in this product are:
- MUPIROCIN (UNII: D0GX863OA5)
- MUPIROCIN (UNII: D0GX863OA5) (Active Moiety)
Which are Mupirocin 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:
- POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
What is the NDC to RxNorm Crosswalk for Mupirocin?
- RxCUI: 106346 - mupirocin 2 % Topical Ointment
- RxCUI: 106346 - mupirocin 0.02 MG/MG Topical Ointment
- RxCUI: 106346 - mupirocin 20 MG per GM Topical Ointment
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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".