NDC 59365-6064 Lugols Strong Iodine
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What is NDC 59365-6064?
What are the uses for Lugols Strong Iodine?
Which are Lugols Strong Iodine UNII Codes?
The UNII codes for the active ingredients in this product are:
- IODINE (UNII: 9679TC07X4)
- IODINE (UNII: 9679TC07X4) (Active Moiety)
- POTASSIUM IODIDE (UNII: 1C4QK22F9J)
- IODIDE ION (UNII: 09G4I6V86Q) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Lugols Strong Iodine?
- RxCUI: 205228 - iodine 5 % / potassium iodide 10 % Topical Solution
- RxCUI: 205228 - iodine 50 MG/ML / potassium iodide 100 MG/ML Topical Solution
- RxCUI: 205228 - Iodine 50 MG/ML / K+ Iodide 100 MG/ML Topical Solution
- RxCUI: 205228 - Iodine 50 MG/ML / Pot Iodide 100 MG/ML Topical Solution
- RxCUI: 205228 - Lugol's strong iodine 5 % / 10 % Topical Solution
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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".