Ultra Pro
Product Images NDC 55924-2001

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Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Ultra Pro (NDC 55924-2001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sena 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.

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FDA Label Image

Ultra Pro Label (Label)

Ultra Pro Label (Label)
This is a product for weight loss and cravings control marketed by SOA. The product consists of a 1 FL OZ (29.6ml) bottle with homeopathics intended for professional use only. The bottle must be shaken and sprayed twice a day under the tongue, avoiding eating, drinking or brushing teeth five minutes before or after. The product is not recommended for children under 15 years old, and pregnant or breastfeeding women should consult a physician before using it. In case of overdose, a Poison Control Center should be contacted immediately. The product should be stored in a cool and dry place. The active ingredients are Abrotanum 10X, Anacard o, 10X, Baryta mur. 10X, Cal, carb. 10X, Caic. phos. 10X, Fucus vesiculosus 10X, Graphites 10K, Hellebor nig. 10X, Hypothalamus 15X, It 10X Lyoopocum 10X, Vagnes ghos 10X Secde 10X Sicaa T0(ofidago virgaurea 10X, Thyroidinum 15X, Thymus serpyllum 10X, whereas the inactive ingredients are USP Purified water, USP Gluten-free, non-GMO, organic cane dispensing alcohol 20%. The information provided has not been reviewed by the Food and Drug Administration.*

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