Dibucaine
Product Images NDC 0168-0046

2 FDA label images from E. Fougera & Co. A Division Of Fougera Pharmaceuticals Inc. · 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 Dibucaine (NDC 0168-0046). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by E. Fougera & Co. A Division Of Fougera 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

Package Label – Principal Display Panel – Label (Dibucaine 01)

Package Label – Principal Display Panel – Label (Dibucaine 01)
Drug facts panel for DIBUCAINE Ointment USP, 1%, a topical anesthetic by E. Fougera & Co., a division of Fougera Pharmaceuticals Inc. The label provides the active ingredient, purpose, uses for temporary pain relief including minor burns and insect bites, warnings for external use, and storage instructions. It states not to use in the eyes and to keep out of reach of children.*
FDA Label Image

Package Label – Principal Display Panel – Carton (Dibucaine 02)

Package Label – Principal Display Panel – Carton (Dibucaine 02)
The image shows the packaging label for DIBUCAINE Ointment USP, 1%, a topical anesthetic by E. Fougera & Co., a division of Fougera Pharmaceuticals Inc. The carton indicates a net weight of 28.35 g (1 oz) and features drug facts, usage warnings, directions, and other information. The label includes a laminate tube with a child-resistant cap, external use warnings, and a barcode with NDC 0168-0046-31.*

* 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.