Docosanol Cream
Product Images NDC 69452-550

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Docosanol (NDC 69452-550). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bionpharma 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

Image1 (Image1)

An instructional illustration showing four steps for using a topical cream container: twisting to open the cap, pressing the pump to dispense cream, applying cream to the fingertip, and closing the container by reattaching the cap.*

FDA Label Image

Tube-carton (Tube Carton)

Packaging label for Docosanol cream 10% topical cream by BIONPHARMA INC. The label features the a+health logo and states it is for cold sore/fever blister treatment. The package contains 2 tubes of 2 g (0.07 oz) each, total net weight 4 g (0.14 oz), labeled as a twin pack. The label highlights that it shortens healing time and duration of symptoms including tingling, pain, burning, and itching. It also notes this is the only FDA approved medicine to shorten healing time. Additional drug facts and directions text is included on the sides of the packaging.*

FDA Label Image

Pump-carton (Pump Carton)

Packaging label for a 2 g (0.07 oz) tube of Docosanol cream 10%, a topical cold sore and fever blister treatment by Bionpharma Inc. The label highlights it as an FDA-approved medicine to shorten healing time, featuring a portable pump dispenser. It includes usage instructions, drug facts, ingredients, warnings, and storage information on a predominantly dark blue background with orange and white text.*

* 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.