Soma Disordergen
FDA Label NDC 58370-4001

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Soma Biotechnology Co., Ltd for the product Soma Disordergen (NDC 58370-4001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding otc - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

coriolus versicolorr


Inactive Ingredient

red ginseng powder, licorice, aralia continentalis, houttuynia cortata, cnidium officinale, cinnamon bark, houttuynia, mulberry leaf, astragalus membranaceus, gigantic angelica, sweet rush, pepper, bongchul, plueropterus multiflorus, dired clove, caramel


Otc - Purpose

To improve blood circulation and immunity, vitalize body parts and produce nerve cells


Otc - Keep Out Of Reach Of Children

keep out of reach of the children


Indications & Usage

■ Take 2 times a day



Warnings

■ do not use if having a cardiac disorder
■ Ask a doctor before taking more than 8 tablets.


Dosage & Administration

for oral use only


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