Vitiligo Liquid
Product Images NDC 55714-2592

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Vitiligo (NDC 55714-2592). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Newton Laboratories, 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.

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FDA Label Image

Package Label (N081 L01)

Package Label (N081 L01)
This product is formulated for symptoms associated with Vitiligo, such as loss of pigmentation, changes in the skin, inflammation, itching, and premature graying. The recommended dosage for ages 12 and up is 6 drops four times daily, while for ages 0 to 11, 3 drops are recommended. The active ingredients include Echinacea, Rumex, Asencum alb., Berberis vulgaris, Bovista, Dalichos, Hydrastis canadensis, Hydrocotyle asiatica, Lycopodium clavatum, Mezereum, Rhus toxicodendron, Rumex crispus, Sepia, Tormacum, Thlapsi bursa-pastoris, and Urtica urens. Inactive ingredients include USP Purified Water, USP Gluten-free, non-GMO, organic cane alcohol 20%.*

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