Product Images Sodium Iodide I 123

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Product Label Images

The following 4 images provide visual information about the product associated with Sodium Iodide I 123 NDC 69945-602 by Curium Us Llc, such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.

Graph 1 - sodium iodide i 123 capsules 69945 1

Graph 1 - sodium iodide i 123 capsules 69945 1

Graph 2 - sodium iodide i 123 capsules 69945 2

Graph 2 - sodium iodide i 123 capsules 69945 2

This text seems to show a table with two rows and seven columns. The first row has the sequential number '1' repeated three times in separate cells. The second row includes numbers representing time values that increase by 5, starting from 0 and ending at 30. The text at the top of the columns reads "Calibration Expiration Time" and "HOURS Time", respectively. It appears to be a chart created to track the calibration expiration time for a particular device.*

Display Panel A601CO - sodium iodide i 123 capsules 69945 3

Display Panel A601CO - sodium iodide i 123 capsules 69945 3

This is a prescription drug called "Sodium Iodide 1123 Capsules" manufactured by "Curum US LC". It is for oral administration only and must be handled only by qualified personnel. The drug must be stored in a container and kept at controlled room temperature (20°C to 25°C). The package insert should be read before use. The drug is radioactive and falls under the regulations of the Nuclear Regulatory Commission and state regulatory agencies. The details of the dosage and expiry date are also given.*

Display Panel A602CO - sodium iodide i 123 capsules 69945 4

Display Panel A602CO - sodium iodide i 123 capsules 69945 4

This is a description of a product called "Sodium iodide 1123 capsules" which is a diagnostic drug that must be handled by qualified personnel due to its radioactive nature. It is manufactured by Curum U LC and should be stored at a controlled room temperature between 20°to25°C (68°to 77°F). There is a warning on the package that the drug should be handled only by qualified personnel in conformity with regulations of the Nuclear Regulatory Commission or state regulatory agencies where applicable. The text also mentions the presence of a total Act MBa/cap (uCi/cap) and an expiration date. The package insert should be read for directions for use and it is for oral administration only. There is no information given about the purpose of the drug or what it is used to diagnose.*

* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.