Pre/post Surgetone Liquid
Product Images NDC 44911-0651

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Pre/post Surgetone (NDC 44911-0651). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Energique, 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.

FDA Label Image

Pre/post Surgetone (Enrg0559 Prepost Surgetone 1 10 22)

Pre/post Surgetone (Enrg0559 Prepost Surgetone 1 10 22)
This is a warning label for a homeopathic remedy called "PRE/POST SURGETONE" by Energique, Inc. It is recommended that pregnant or breastfeeding individuals consult with a healthcare professional before using this product. It should also be kept out of reach of children and stored in a cool, dry place. This remedy claims that it may temporarily relieve soreness after overexertion, pain, and soreness after procedures, and pain and soreness after an injury and trauma based on traditional homeopathic practice and not on FDA evaluated evidence. The active ingredients for this product are Arica Montana, Calendula Officinalis, Hypericum Perforatum, Phosphorus, Rhus Tox, Staphysagria, and Symphytum Officinale present in 12.50% (in each drop) with other Inactive ingredients. Adults and children over 5 years old are recommended to take 10 drops orally, three times daily, or as directed by healthcare professionals. In case of overdose, medical help should be sought right away, and in case of the tamper-evident seal being broken or missing, the product should not be used. Lot and manufacturing date information are also provided.*

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