Zzip Cold Sore Treatment
Product Images NDC 70019-100

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Zzip Cold Sore Treatment (NDC 70019-100). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zzip Ag, 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

Label1 (Label Pdp)

Packaging label for Zzip Cold Sore Treatment by Zzip AG. The label features the product name and states it relieves pain and halts itching. It shows an image of a woman applying the treatment to her lip. The label also includes the product weight of 0.1 oz (3 ml) and lists Allantoin, Dimethicone, and Menthol as ingredients. The label promotes cold sore, fever blister treatment, and lip protectant use.*

FDA Label Image

Label2 (Label Drugfacts)

Drug Facts panel for Zzip Cold Sore Treatment with active ingredients allantoin 0.5%, dimethicone 1%, and menthol 0.1%. It details uses for cold sore/fever blister relief, warnings, directions for adults and children 12 years and older, and other information including storage instructions and inactive ingredients listing.*

FDA Label Image

Label3 (Label Insert)

Drug Facts label for Zzip Cold Sore Treatment by Zzip AG. The label details its use as a cold sore/fever blister treatment and lip protectant, instructions for application, warnings, active ingredients (Allantoin 0.5%, Dimethicone 1%, Menthol 0.1%), and inactive ingredients. It includes step-by-step directions with illustrations for washing, preparing, applying, disposing, and washing post-application. Storage and contact information are also provided.*

* 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.