Lidocaine Hydrochloride Solution
Product Images NDC 68094-081

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 Hydrochloride (NDC 68094-081). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Precision Dose, 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

Carton Label (Case (ek6319 00))

Carton Label (Case (ek6319 00))
Packaging label for Lidocaine HCl Injection, USP 2% (100 mg/5 mL or 20 mg/mL) solution for intravenous use. The label shows a box containing 25 single-dose vials of 5 mL each. It highlights that the product is methylparaben free, intended for infiltration and nerve block including caudal and epidural use, and is manufactured for Precision Dose, Inc. The NDC is 68094-081-25.*
FDA Label Image

Vial Label (Label (el6670 00))

Vial Label (Label (el6670 00))
Label for Lidocaine Hydrochloride Injection USP 2% solution, 100 mg/5 mL (20 mg/mL) in a 5 mL single-dose vial. The label states it is sterile, nonpyrogenic, and methylparaben free. The product is for infiltration and nerve block including caudal and epidural use. Labeled by Precision Dose, Inc. with NDC 68094-081-01. Storage instructions specify 20 to 25°C (68 to 77°F).*
FDA Label Image

Formula (Figure 1)

Formula (Figure 1)
Chemical structure of lidocaine hydrochloride, showing its molecular formula arrangement with aromatic ring, amino group, and hydrochloride moiety as depicted in the image.*

* 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.