Lidocaine 5%
Product Images NDC 17856-0028

3 FDA label images from Atlantic Biologicals Corp. · 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 5% (NDC 17856-0028). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Atlantic Biologicals Corp., 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

Image Description (17856 0028 01)

Image Description (17856 0028 01)
Label for Lidocaine Ointment USP 5%, 1 mL, supplied in a quantity of 120 syringes. The label includes storage instructions, usage warning (for topical use only, do not use in eyes), dosage information, packaging and distribution details by Atlantic Biologicals Corp. The product is identified with NDC 17856-0028-01.*
FDA Label Image

Formula (Chemical Layout)

Formula (Chemical Layout)
Chemical structure of Lidocaine showing its molecular components, including aromatic ring with two methyl groups, amide linkage, and diethylamino group.*
FDA Label Image

Drug Interaction Chart 1 (Drug Associated With Mm1)

Drug Interaction Chart 1 (Drug Associated With Mm1)
A data table listing drug classes and example drugs within each category. Classes include Nitrates/Nitrites, Local anesthetics, Antineoplastic agents, Antibiotics, Antimalarials, Anticonvulsants, and Other drugs, with examples such as nitroglycerin, lidocaine, cyclophosphamide, dapsone, chloroquine, phenytoin, and acetaminophen respectively.*

* 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.