Lidocaine Hydrochloride Solution
Product Images NDC 73293-0001

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Lidocaine Hydrochloride (NDC 73293-0001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Huons Co., Ltd., 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

Figure 1 (Figure 1)

Chemical structure diagram of Lidocaine Hydrochloride, showing the molecular components including aromatic ring with methyl groups, amide linkage, and side chains with ethyl groups, associated with HCl and water molecules.*

FDA Label Image

Ek5754-05 (Ek5754 05)

Label for Lidocaine HCl Injection, USP 1% (10 mg/mL) solution, supplied in 10 single-dose vials of 5 mL each. The label states it is methylparaben-free and intended for infiltration and nerve block including caudal and epidural use. Manufactured by Huons Co., Ltd., Korea. Includes dosage ingredient details, storage instructions, a barcode, and a warning to sell only as an unbroken package.*

FDA Label Image

El5938-05 (El5938 05)

Label for Lidocaine HCl Injection, USP 1% solution containing 50 mg/5 mL (10 mg/mL) in a 5 mL single dose vial. The label states it is for infiltration and nerve block including caudal and epidural use, is methylparaben free, and is Rx only. The product is labeled by Huons Co., Ltd. and includes an NDC 73293-0001-1 barcode.*

FDA Label Image

Ek6155-02 (Ek6155 02)

Packaging label for Lidocaine HCl Injection, USP 2% solution (20 mg/mL) in 5 mL single-dose vials. The label indicates methylparaben-free formulation and is manufactured by Huons Co., Ltd. The package contains 10 vials and highlights use for infiltration and nerve block including caudal and epidural use. Storage and dosage instructions are printed on the label, alongside a barcode and NDC 73293-0003-2.*

FDA Label Image

El6469-01 (El6469 01)

Label for Lidocaine HCl Injection, USP 2% solution containing 100 mg/5 mL (20 mg/mL) in a 5 mL single-dose vial by Huons Co., Ltd. The label includes usage for infiltration and nerve block including caudal and epidural use, and notes methylparaben free. It also shows the NDC number 73293-0003-1.*

FDA Label Image

Ek6235-00 (Ek6235 00)

Label for Lidocaine HCl Injection, USP solution 1% (10 mg/mL), 200 mg/20 mL multiple dose vials. The label includes composition details, usage instructions specifying infiltration and nerve block, cautions on use, storage conditions, and manufacturing information by Huons Co., Ltd. The packaging has green and white colors with some Korean text on the side.*

FDA Label Image

El6597-00 (El6597 00)

Label for Lidocaine HCl Injection, USP 1% solution, containing 200 mg per 20 mL (10 mg/mL) in a 20 mL multiple dose vial. The label notes usage for infiltration and nerve block, excluding caudal and epidural use. It is a sterile, nonpyrogenic solution manufactured by Huons Co., Ltd. Storage conditions and caution statements are included along with the NDC 73293-0004-1 barcode.*

FDA Label Image

Ek6236-00 (Ek6236 00)

Box packaging label for Lidocaine HCl Injection, USP 2% solution (20 mg/mL) with a total content of 400 mg/20 mL. The label specifies it is sterile and nonpyrogenic, containing lidocaine HCl, sodium chloride, methylparaben, and pH adjusted with sodium hydroxide and/or hydrochloric acid. It is for intravenous use, manufactured by Huons Co., Ltd., and sold as multiple 20 mL vials. The label includes storage instructions and a barcode.*

FDA Label Image

El6598-00 (El6598 00)

Lidocaine HCl Injection, USP 2% (20 mg/mL) solution, 400 mg/20 mL multiple dose vial by Huons Co., Ltd. Label states it is for infiltration and nerve block, not for caudal and epidural use, sterile and nonpyrogenic, with storage instructions and a barcode.*

* 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.