Opitox Topical
Product Images NDC 72380-521

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Opitox Topical (NDC 72380-521). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Vivera Pharmaceuticals, Inc., 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

Opitox Box (Opitox Box)

OPITOX Topical Gel packaging label from Vivera Pharmaceuticals, Inc. The label shows the product name, indicates it is a topical gel for pain relief, and displays images of people holding painful areas. The box contains 3 fluid ounces (88.7 mL) of the gel. The label includes the Drug Facts panel, usage instructions, warnings, and active ingredients such as menthol and camphor. Manufacturer and contact information are also visible.*

FDA Label Image

Opitox Pip (Opitox Pip)

OPITOX Topical Gel by Vivera Pharmaceuticals, Inc. is shown, featuring a white box and tube with blue and black text. The packaging highlights "Pain Relief" and a wave design in blue. The box and tube display the product name, labeler, NDC number 72380-521, and emphasize topical analgesic use.*

FDA Label Image

Opitox Tube (Opitox Tube)

Label for OPITOX TOPICAL Gel by Vivera Pharmaceuticals, Inc., presented in a 3.0 fl oz (88.7 mL) tube. The label highlights the product as a topical pain relief gel. The active ingredients and drug facts are clearly displayed on the label. Manufactured by Soba Medical, a subsidiary of Vivera Pharmaceuticals based in Santa Fe Springs, CA. The label includes usage and safety information along with the product's chemical structure background graphic.*

* 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.