Product Images Acetaminophen

View Photos of Packaging, Labels & Appearance

Product Label Images

The following 4 images provide visual information about the product associated with Acetaminophen NDC 36000-306 by Baxter Healthcare Corporation, 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.

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The text appears to be a graph or table displaying the mean temperature values in Celsius over time (in hours) after a dose of either acetaminophen or a placebo. There are two lines on the graph, one representing the acetaminophen group and the other representing the placebo group.*

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This text is a set of instructions for using Acetaminophen Injection in a clinical setting. The injection is for intravenous use only and comes in a single dose container, which must be discarded if there is any unused portion. Aseptic transfer is required for doses greater than 1,000 mg. The package insert contains the recommended dosage and full prescribing information. Acetaminophen Injection should be stored at controlled room temperature and should not be refrigerated or frozen. Before use, check the container for minute leaks. Each 100 mL of the injection contains 1,000 µg of acetaminophen with other pharmaceutical ingredients. The VIAFLO container used for the product is free from natural rubber latex, DEHP, or VC.*

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This is a description of a single dose container of Acetaminophen Injection for intravenous use only. The container has a volume of 100mL and the NDC number is 36000-306-60. The package insert should be consulted for recommended dosage and full prescribing information. The solution must be stored at a controlled room temperature and not be refrigerated or frozen. If leaks are found, the solution should be discarded. Each 100 mL contains 1,000 mg acetaminophen, USP, 3,850 mg ‘manitol, USP, 25 mg L-cysteine hydrochloride monohydrate, USP, and 10.4 mg dibasic sodium phosphate anhydrous, USP. The manufacturing date and the expiry date can be found on the solution container.*

* 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.