Sunmark Benzoin Compound Tincture Liquid
Product Images NDC 49348-138

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Sunmark Benzoin Compound Tincture (NDC 49348-138). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Strategic Sourcing Services 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

Smbenz.jpg (Smbenz)

Sunmark Benzoin Compound Tincture NFXI topical liquid with 79% alcohol, 2 FL OZ (59 mL) bottle. The label identifies it as an oral mucosal protectant and cautions about warnings, directions, and inactive ingredients. Distributed by McKesson, San Francisco, CA.*

FDA Label Image

Sunmark Benzoin Tincture.jpg (Sunmark Benzoin Tincture)

Sunmark Benzoin Compound Tincture NFXI 79% Alcohol topical liquid in a 2 FL OZ (59 mL) bottle. The label highlights its use as an oral mucosal protectant containing 1000 mg/mL Benzoin Resin. It includes directions, warnings, active and inactive ingredients, storage instructions, and a barcode. The product is labeled by Strategic Sourcing Services LLC.*

* 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.