NDC 11960-0049 Nitrotan
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 11960-0049?
What are the uses for Nitrotan?
Which are Nitrotan UNII Codes?
The UNII codes for the active ingredients in this product are:
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ISOPROPYL ALCOHOL (UNII: ND2M416302) (Active Moiety)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- BENZYL ALCOHOL (UNII: LKG8494WBH) (Active Moiety)
- PICRIC ACID (UNII: A49OS0F91S)
- PICRIC ACID (UNII: A49OS0F91S) (Active Moiety)
- TANNIC ACID (UNII: 28F9E0DJY6)
- TANNIC ACID (UNII: 28F9E0DJY6) (Active Moiety)
Which are Nitrotan 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:
- ISOBUTANE (UNII: BXR49TP611)
- PROPANE (UNII: T75W9911L6)
What is the NDC to RxNorm Crosswalk for Nitrotan?
- RxCUI: 1432138 - benzyl alcohol 6.1 % / isopropyl alcohol 62 % / picric acid 0.2 % / tannic acid 1.5 % Topical Spray
- RxCUI: 1432138 - benzyl alcohol 0.061 ML/ML / isopropyl alcohol 0.62 ML/ML / picric acid 2 MG/ML / tannic acid 15 MG/ML Topical Spray
- RxCUI: 1432143 - Nitrotan 62 % / 6.1 % / 1.5 % / 0.2 % Topical Spray
- RxCUI: 1432143 - benzyl alcohol 0.061 ML/ML / isopropyl alcohol 0.62 ML/ML / picric acid 2 MG/ML / tannic acid 15 MG/ML Topical Spray [Nitrotan]
- RxCUI: 1432143 - Nitrotan (benzyl alcohol 6.1 % / isopropyl alcohol 62 % / picric acid 0.2 % / tannic acid 1.5 % ) Topical Spray
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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".