Lidocaine Ointment
Product Images NDC 62332-424

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Lidocaine (NDC 62332-424). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Alembic Pharmaceuticals 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 diagram of lidocaine showing its molecular configuration with labeled functional groups and atoms.*

FDA Label Image

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The packaging label for Lidocaine Ointment USP 5%, a topical ointment containing 50 mg/g lidocaine. The label states it is for prescription use only and warns not to use in the eyes. It includes storage instructions and dosage directions. Manufactured for Alembic Pharmaceuticals Inc., USA, and by Aleor Dermaceuticals Ltd., India. The package contains a 30 g laminate tube with a child-resistant cap. NDC 62332-424-30 is visible on the label.*

FDA Label Image

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Packaging label for Lidocaine Ointment USP 5%, topical ointment with a net weight of 35.44 g (1¼ Oz). Labeler is Alembic Pharmaceuticals Inc. The label includes usage warnings, manufacturer details for Aleor Dermaceuticals Ltd. India, child-resistant cap instructions, batch coding, and barcodes. The label states it is Rx only and highlights that the ointment is for topical use only, not for use in eyes.*

FDA Label Image

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Label for Lidocaine Ointment USP, 5%, topical ointment in a 50g wide-mouth jar with child-resistant cap. Contains the active ingredient lidocaine base 5% and instructions for use, storage, and warnings. Manufactured by Alembic Pharmaceuticals Inc., with barcode and batch coding information included.*

* 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.