Vitiligo
Product Images NDC 55714-2350

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Vitiligo (NDC 55714-2350). 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 001 001)

Package Label (N081 L01 001 001)
This is a description of a product called "Vitiligo" that is formulated to address skin related issues such as pigmentation loss, changes in the skin, inflammation, itching, and premature graying. It comes in a 1 fl oz (29.57 ml) bottle and is meant for oral use only. The ingredients include Beech Drops, Black Cohosh, Dolomite, Graphites, Lycopodium clavatum, Natrium muriaticum, Rhus toxicodendron, Sulphur, and Thuja occidentalis. The directions mention shaking well before use and taking several drops orally. The product has both active and inactive ingredients with names such as US Porfe wi, LS G-z, and silicone dispersing kol, among others. There is also a mention of a Stockt NOBY Lottt.*

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