Proparacaine Hydrochloride Solution/ Drops
Product Images NDC 70756-193

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 Proparacaine Hydrochloride (NDC 70756-193). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lifestar Pharma Llc, 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

Proparacaine Hydrochloride Molecular Structure Representation (7d7eab12 F721 4092 8c18 7100544ade2b 01)

Proparacaine Hydrochloride Molecular Structure Representation (7d7eab12 F721 4092 8c18 7100544ade2b 01)
Chemical structure of Proparacaine hydrochloride showing its molecular formula (C16H26N2O3 ยท HCl), molecular weight (MW 330.85), and CAS number (5875-06-9). The diagram displays the chemical bonds and components of the molecule.*
FDA Label Image

Label (7d7eab12 F721 4092 8c18 7100544ade2b 02)

Label (7d7eab12 F721 4092 8c18 7100544ade2b 02)
Label for Proparacaine Hydrochloride Ophthalmic Solution USP 0.5% (5 mg/mL), sterile, 15 mL drops. The product is for eye use only and prescription use only (Rx only). It is manufactured by Lifestar Pharma LLC and is a product of Switzerland. The label lists inactive ingredients, storage instructions, precautions, and tamper-evident seal warnings.*
FDA Label Image

Carton (7d7eab12 F721 4092 8c18 7100544ade2b 03)

Carton (7d7eab12 F721 4092 8c18 7100544ade2b 03)
Proparacaine Hydrochloride Ophthalmic Solution, USP 0.5% sterile eye drops in a 15 mL bottle, labeled for prescription use only. The packaging indicates storage instructions, usage precautions, and lists inactive ingredients and preservatives. Manufactured for Lifestar Pharma LLC, the product is for ophthalmic administration, with labeling that includes the NDC 70756-193-35 and is marked as sterile.*

* 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.