Xodol
Product Images NDC 42254-114

3 FDA label images from Rebel Distributors Corp · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Xodol (NDC 42254-114). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rebel Distributors Corp, 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

Hydrocodone Bitartrate Chemical Structure (5b50291b 68c7 45a6 Ae38 59f137ca7620 01)

Hydrocodone Bitartrate Chemical Structure (5b50291b 68c7 45a6 Ae38 59f137ca7620 01)
Chemical structure diagram depicting the active ingredient in Xodol, including its molecular configuration and associated hydrate form (2 1/2 H2O). The structure shows a complex arrangement of carbon, hydrogen, and oxygen atoms characteristic of the compound.*
FDA Label Image

Acetaminophen Chemical Structure (5b50291b 68c7 45a6 Ae38 59f137ca7620 02)

Acetaminophen Chemical Structure (5b50291b 68c7 45a6 Ae38 59f137ca7620 02)
Chemical structure of the active ingredient in Xodol by Rebel Distributors Corp, showing a phenol ring bonded to an acetamide group with a hydroxyl substituent.*
FDA Label Image

Xodol 7.5mg/300mg (5b50291b 68c7 45a6 Ae38 59f137ca7620 03)

Xodol 7.5mg/300mg (5b50291b 68c7 45a6 Ae38 59f137ca7620 03)
Xodol 7.5mg/300mg tablets label for a #60 count bottle by Rebel Distributors Corp. Each tablet contains hydrocodone bitartrate 7.5mg and acetaminophen 300mg. The label includes warnings about habit formation, Product ID QX011460, and dosing instructions. It is packaged by Physician Partner, Thousand Oaks, CA, with storage instructions for controlled room temperature (15°-30°C). The NDC is 42254-114-60.*

* 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.