Body Pure
FDA Label NDC 50114-4426

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Heel Inc for the product Body Pure (NDC 50114-4426). 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 keep out of reach of children, indications and usage, warnings, dosage and administration, active ingredient, inactive ingredient, purpose, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Keep Out Of Reach Of Children

Keep this and all medicines out of the reach of children.

Indications And Usage

For the temporary relief of:
  • Fatigue
  • Mild Skin Rashes
  • Nausea and Headaches

Warnings

If symptoms persist or worsen, a physician should be consulted. As with any drug, if you are pregnant or nursing a baby, seek the advise of a health care professional before using this product.

Dosage And Administration

Adults and children above 6 years: 1 tablet sublingually or dissolved completely in mouth 3 times daily of as directed by a physician. Infants and children to 6 years: 1/2 the adult dosage.

Active Ingredient

Each 300mg tablet contains as active ingredients: a-Lipicum 3X, Avena saltvia 3X, Ricinus communis 3X, Solidago vigaurea 4X, Viola tricolor 4X, Berberis vulgaris 6X, Caffeinum 6X, Juglans regia 6X, Rhamus purshiana 6X, Urtica urens 6X, Cholesterium 10X, Influenzium 12X, Petroleum 12X, Tabacum 12X, X-ray 12X, Nux vomica 30x 16.67 mg

Inactive Ingredient

Inactive ingredients: Lactose, Magnesium Sterarate

Purpose

Fatigue, Mild Skin Rashes, Nausea, and Headaches

* Please review the disclaimer below.