Lv-fx Liquid
FDA Label NDC 64616-097

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Vitality Works, Inc for the product Lv-fx (NDC 64616-097). 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 lv-fx, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Lv-Fx

Aesculus Hippocastanum 10X                 Carduus Marianus 15X                 Ruta Graveolens 10X

Anacardium Occidentale 14X                   Cedron 9X                                   Selenium Metallicum 15X, 30X

Aralia Racemosa 10X                              Helonias Dioica 10X                     Sumbul 14X

Arsenicum Album 13X                             Ledum Palustre 10X, 20X             Thyroidinum 6C

Arsenicum Iodatum 13X                         Manganum Aceticum 20X              Veratrum Viride 6X

Bellis Perennis 7X                                   Myrtus Communis 2X

Calcarea Fluorica 10X, 20X                    Physalis Alkekengi 5X

Acohol, Purified Water

Use only under the direction of a health care professional. Do not use if tamper evident seal is broken or missing.

Keep out of reach of children. In case of overdose, get medical help or contact Poison Control Center right away.

For the temporary relief of digestive upset, symptoms of food allergies and nausea.

Orally 25 drops, 2 times per day or as indicated by a physician. Children 12 and under use one half the adult dosage.

Aids in liver function.

* Please review the disclaimer below.