Lidocaine Ointment
Product Images NDC 85509-1418

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 (NDC 85509-1418). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Phoenix Rx Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Label (8550914183)

Label (8550914183)
This text provides information about a medication with NDC# 85509-1418-3, containing Lidocaine USP base 5% in a water-soluble base of polyethylene glycol 400 and polyethylene glycol 1450. It is an ointment meant for topical use only. The usual dosage instructions are available in the package insert. The warning advises keeping the product out of reach of children and not using it in the eyes. Storage should be at 20° to 25°C (68° to 77°F), with excursions permitted to 15° to 30°C (59° to 86°F) according to USP Controlled Room Temperature guidelines. The product is Rx only and manufactured by Glenmark Pharmaceuticals Limited, with relabeling by PHOENIX RX LLC. Additional information includes the GTIN, SN, LOT number, and expiration date.*
FDA Label Image
Glenmark Logo (Glenmark Logo)
FDA Label Image

Structure (Structure)

Structure (Structure)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.