Crane Safety Xs Non-aspirin Tablet, Film Coated
Product Images NDC 73408-904

2 FDA label images from Crane Safety Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Crane Safety Xs Non-aspirin (NDC 73408-904). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Crane Safety Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

C1 Xs (C1 Xs Non Aspirin Label 11)

C1 Xs (C1 Xs Non Aspirin Label 11)
This image displays the Drug Facts and packaging information for Crane Safety XS Non-Aspirin extra strength tablets. The active ingredient is acetaminophen 500 mg per tablet, used as a pain reliever and fever reducer. The label includes usage instructions, warnings about liver damage, allergy alerts, dosage directions for adults and children, and inactive ingredients. It also features cautionary notes, storage directions, and company contact information for Crane Safety LLC.*
FDA Label Image

C2 Xs (C2 Xs Non Aspirin Label 11)

C2 Xs (C2 Xs Non Aspirin Label 11)
Drug Facts text panel for Crane Safety XS Non-Aspirin 500 mg tablets includes sections on active ingredient (acetaminophen 500 mg), uses for pain relief and fever reduction, warnings about liver damage and allergies, directions for use including adult and child dosing, other storage and usage information, inactive ingredients list, and contact information for questions or comments. The panel also emphasizes the package is for households without young children and notes tamper-evident sealed packets with 100 tablets.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.