Lidocaine Hydrochloride Jelly
Product Images NDC 0404-9898

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Lidocaine Hydrochloride (NDC 0404-9898). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Henry Schein, 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

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Chemical structure of Lidocaine Hydrochloride illustrating its molecular configuration with aromatic and amide components, ethyl groups, and associated hydrochloride.*

FDA Label Image

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An instructional illustration showing syringe assembly directions for Lidocaine Hydrochloride 20 mg/mL jelly. The steps include opening a sterile pouch to place contents on a sterile field, threading the vial into the injector 3 half turns without pushing it in to avoid misalignment, and removing the cap to expel air before use. Each step is accompanied by a simple line drawing.*

FDA Label Image

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Data table listing stock numbers and packaging details for different sizes of Lidocaine Hydrochloride jelly, including 5 mL, 10 mL, and 20 mL sizes, with mention of unit use packages containing single-use vials and a URO-JET AC vial injector, packaged in boxes of 25.*

FDA Label Image

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Lidocaine Hydrochloride Jelly 20 mg/mL (2%) topical jelly label. The label indicates a 10 mL package with sterile, single-use jelly for topical anesthetic use. It is manufactured and packaged by Henry Schein, Inc. The label includes storage instructions, lot and expiration information placeholders, and notes that no preservatives are added.*

* 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.