Lidocaine Hydrochloride Jelly
Product Images NDC 0404-9899

View Photos of 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 Lidocaine Hydrochloride (NDC 0404-9899). 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

Formula1.jpg (Formula1)

Formula1.jpg (Formula1)
Chemical structure of lidocaine hydrochloride, showing the molecular arrangement of its atoms including aromatic ring, methyl groups, and hydrochloride component.*
FDA Label Image

Image1.jpg (Image1)

Image1.jpg (Image1)
Instructions diagram for syringe assembly and use with vial and URO-JET injector. Includes steps: open sterile pouch and drop contents onto sterile field; thread vial into injector 3 half turns without pushing vial in; remove cap and expel air. Contains caution about improper engaging causing glass breakage and injury.*
FDA Label Image

Label1.jpg (Label1)

Label1.jpg (Label1)
Label for Lidocaine Hydrochloride Jelly 2% (20 mg/mL), 20 mL sterile topical gel. The label indicates the product is for topical use only, preservative-free, sterile in original packaging, single-use, and should be stored at controlled room temperature. Packaged by Henry Schein, Inc. with NDC 0404-9899-20. The label includes barcode, lot, and expiration placeholders along with a QR code and instructions to see the manufacturer's insert for full prescribing information.*

* 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.