Lidocaine Ointment
Product Images NDC 72189-211

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Lidocaine (NDC 72189-211). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Direct Rx, 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

16835 (72189 0168 35)

16835 (72189 0168 35)
LIDOCAINE OINTMENT 5%, topical ointment containing lidocaine base 5% in a water-soluble base with polyethylene glycol 300 and 400. The label displays the net weight of 35.44 grams, lot number, expiration date, and is labeled by DIRECT RX. Multiple NDC numbers are listed for the 5% strength ointment.*
FDA Label Image

72189 0208 50

72189 0208 50
Lidocaine Ointment 5% 50 g tube label displaying the active ingredient Lidocaine base 5% in a water-soluble base with polyethylene glycol 300 and 1450. The label shows the lot number, expiration date, packaging details, and is distributed by Direct Rx. The label includes cautionary and storage instructions along with barcode and NDC information.*
FDA Label Image

72189 0211 50

72189 0211 50
Label for Lidocaine Ointment 5% in a 50 g tube, indicated as a topical human prescription drug. The label includes the active ingredient concentration as Lidocaine USP 5% and lists inactive ingredients such as propylene glycol and polyethylene glycol 3350. It shows the lot number, expiration date, and is packaged and distributed by Direct Rx.*
FDA Label Image

165 (72189 165)

165 (72189 165)
LIDOCAINE OINTMENT 5% topical ointment, 35.44 g tube, packaged and distributed by DIRECT RX. The label includes generic ingredient information noting each gram contains Lidocaine USP 5% in a water-soluble base with polyethylene glycol 400, 3350, and propylene glycol. The NDC code is 72189-165-35, and the lot number and expiration date are also shown.*

* 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.