Benzoin Compound Tincture
Product Images NDC 54162-100

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Benzoin Compound Tincture (NDC 54162-100). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Geritrex 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

1oz (Tb1c Page 001)

Label for Benzoin Compound Tincture U.S.P. by Geritrex LLC, a 1 fl. oz (29 ml) topical protectant containing 77% alcohol. The label highlights its use for protecting skin, oral mucosa, and minor wounds, including under adhesive tape, casts, dressings, and orthodontic appliances. It includes Drug Facts detailing active ingredient, purpose, usage warnings, directions, and company contact information with barcode.*

FDA Label Image

2oz (Tb2)

Drug Facts panel for Benzoin Compound Tincture U.S.P. by Geritrex Corporation, listing the active ingredient as Tincture Benzoin compound USP 100% for skin protectant use. The panel includes warnings, directions for use, storage information, and caution about flammability. It specifies the tincture contains alcohol 77%, aloe, benzoin, storax, and tolu balsam, and is intended to maintain skin integrity and protect from adhesives and harsh body fluids.*

FDA Label Image

4oz (Tb4c Page 001)

Drug Facts panel for Benzoin Compound Tincture U.S.P. showing active ingredient as Tincture Benzoin compound USP 100% with a purpose as skin protectant. It includes intended use, warnings, usage directions, and storage information. Also visible is a protectant usage section indicating 77% alcohol content and flammability, with labeler contact details for Geritrex Corporation.*

* 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.