Sunmark Witch Hazel Liquid
Product Images NDC 49348-181

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Sunmark Witch Hazel (NDC 49348-181). 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

Smwitch.jpg (Smwitch)

This is a drug facts label with information about a product intended to be used for foot irritations and blisters. The active ingredient is Asrgon and the product is an astringent. It contains alcohol and some inactive ingredients. The label provides directions for use and advises users to see a doctor if their symptoms worsen. The product is distributed by Ekesson, and there is a money-back guarantee.*

FDA Label Image

Principal Display Panelndc 49348-181-38witchhazelalcohol 14%16 Fl Oz (1 Pt) 473 mL (Sunmark Witch Hazel 01)

This is a product label, likely for a topical solution indicated for minor skin irritations such as cuts, scrapes, and insect bites. It contains 14% alcohol and is only for external use. The product warns not to get it in the eyes and to seek medical attention if contact occurs; and to stop using it and see a doctor if the condition persists or worsens after 7 days. The product is distributed by McKesson and comes with a money-back guarantee. There are also warning messages not to use the product on broken skin or around the eyes, to keep it away from children, and directions to apply liberally to the affected area as often as needed.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.