NDC 72934-2137 Levocetirizine Dihydrochloride 2% / Mupirocin 2% / Triamcinolone Acetonide 0.025%
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What is NDC 72934-2137?
Which are Levocetirizine Dihydrochloride 2% / Mupirocin 2% / Triamcinolone Acetonide 0.025% UNII Codes?
The UNII codes for the active ingredients in this product are:
- LEVOCETIRIZINE DIHYDROCHLORIDE (UNII: SOD6A38AGA)
- LEVOCETIRIZINE (UNII: 6U5EA9RT2O) (Active Moiety)
- MUPIROCIN (UNII: D0GX863OA5)
- MUPIROCIN (UNII: D0GX863OA5) (Active Moiety)
- TRIAMCINOLONE ACETONIDE (UNII: F446C597KA)
- TRIAMCINOLONE ACETONIDE (UNII: F446C597KA) (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".