Glydo- Lidocaine Hydrochloride Jelly
Product Images NDC 51662-1652

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Glydo- Lidocaine Hydrochloride Jelly (NDC 51662-1652). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co. Llc, Dba Healthfirst, 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

Carton Label (51662 1652 1 Carton Label)

Label of GLYDO lidocaine hydrochloride jelly 20 mg/mL (2%) in a 6 mL single-dose prefilled syringe. The topical anesthetic is sterile and preservative-free. The label includes dosage information, storage instructions, manufacturer (Sagent Pharmaceuticals, Germany), lot and expiration date fields, and barcode.*

FDA Label Image

Rfid Label (51662 1652 1 Rfid)

A white rectangular label featuring printed alphanumeric codes and a small QR code on the right side. Text includes manufacturing and distribution information, noting HF Acquisition Co. LLC, Mukilteo, WA, and a designation for prescription use (RX ONLY). No proprietary or strength details are visible on the label itself.*

FDA Label Image

Table (51662 1652 1 Table 1)

A table listing drug classes alongside examples of drugs within each class. Classes include Nitrates/Nitrites, Local anesthetics, Antineoplastic Agents, Antibiotics, Antimalarials, Anticonvulsants, and Other drugs, with corresponding examples like lidocaine under Local anesthetics and chloroquine under Antimalarials.*

FDA Label Image

Structure (51662 1652 1 Structure)

Chemical structure diagram of lidocaine hydrochloride, showing the molecular arrangement of atoms including aromatic ring, amide group, and diethylamino group linked to hydrochloride.*

* 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.