Lipocaine 5 Cream
Product Images NDC 63135-811

3 FDA label images from Esba Laboratories Inc. · 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 Lipocaine 5 (NDC 63135-811). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Esba Laboratories 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

Outer Carton Lipocaine 5 (30 g tube)

Outer Carton Lipocaine 5 (30 g tube)
The packaging label for LIPOCAINE 5 Topical Anesthetic Cream, containing lidocaine 5% in liposomes. The label highlights features such as being alcohol-free and non-stinging. It displays the net weight of 1 oz (30 grams), manufacturer ESBA Laboratories Inc., and includes drug facts, usage directions, inactive ingredients, and a barcode. The design features blue, beige, and green elements with emphasis on fast skin numbing and a 100% vegan naturally derived vehicle.*
FDA Label Image

Lipocaine 5- Tube 113 Grams Label (Labels Lipocaine 4 Oz 5 By 4.45 Rev1 X1200 Fda)

Lipocaine 5- Tube 113 Grams Label (Labels Lipocaine 4 Oz  5 By 4.45 Rev1 X1200 Fda)
Label for LIPOCAINE 5 Lidocaine 5% topical anesthetic cream by ESBA Laboratories Inc. Packaging highlights lidocaine in liposomes for fast and deep skin numbing. The cream is alcohol free, vegan, and contains naturally derived ingredients. Net weight is 4 ounces (113 grams). The label includes a detailed Drug Facts panel and directions for use.*
FDA Label Image

Label Lipocaine 5 (30 g tube)

Label Lipocaine 5 (30 g tube)
Label of LIPOCAINE 5 topical anesthetic cream, containing Lidocaine 5% w/w in liposomes. The label shows product name, strength, dosage form (cream), net weight 1 oz (30 grams), manufacturer ESBA Laboratories Inc., and product NDC 63135-811-30. It includes drug facts highlighting active ingredient, uses for temporary relief of pain and itching due to anorectal disorders, warnings, flammability caution, and usage directions.*

* 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.