Lidocaine Hydrochloride Solution
Product Images NDC 0121-0972

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 Hydrochloride (NDC 0121-0972). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pai Holdings, Llc Dba Pai Pharma, 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

Lido-nomenclature (Lidocaine Hydrochloride Topical Solution Usp Fn 0 1)

Lido-nomenclature (Lidocaine Hydrochloride Topical Solution Usp  Fn 0 1)
Chemical structure of Lidocaine Hydrochloride, showing its molecular composition with labeled functional groups including amide, aromatic ring with methyl substituents, and the hydrochloride salt.*
FDA Label Image

Pai Logo Wa (Lidocaine Hydrochloride Topical Solution Usp Fn 0 2)

FDA Label Image

Pai Logo (Lidocaine Hydrochloride Topical Solution Usp Fn 0 3)

Pai Logo (Lidocaine Hydrochloride Topical Solution Usp  Fn 0 3)
Lidocaine Hydrochloride 40 mg/mL topical solution label from PAI Holdings, LLC dba PAI Pharma. The label features the PAI Pharmaceutical Associates, Inc. logo and company information based in Greenville, SC. No additional dosage or packaging details are visible.*
FDA Label Image

50 mL- Lido Bottle Label (Lidocaine Hydrochloride Topical Solution Usp Fn 0 4)

50 mL- Lido Bottle Label (Lidocaine Hydrochloride Topical Solution Usp  Fn 0 4)
Label for Lidocaine Hydrochloride Topical Solution USP 4% (40 mg/mL) in a 50 mL bottle. The label specifies the product is for topical use only, not for injection, and includes storage instructions and warnings. Labeled by PAI Holdings, LLC dba PAI Pharma.*

* 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.