Heavy Metal Detox Liquid
FDA Label NDC 55714-2455

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Newton Laboratories, Inc. for the product Heavy Metal Detox (NDC 55714-2455). 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 indications & usage section, dosage & administration section, otc - active ingredient section, otc - purpose section, inactive ingredient section, questions section, warnings section, otc - pregnancy or breast feeding section, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Indications & Usage Section

Formulated for associated symptoms such as fatigue, headaches, oversensitivity and sluggish elimination.

Dosage & Administration Section

Directions: Ages 12 and up, take 6 drops by mouth (ages 0 to 11, give 3 drops) one to four times daily or as directed by a health professional. Sensitive persons begin with 1 drop and gradually increase to full dose.

Otc - Active Ingredient Section

Equal parts of Iris versicolor 6x, Taraxacum officinale 6x, Allium sativum 15x, Aluminium metallicum 15x, Argentum metallicum 15x, Aurum metallicum 15x, Baryta carbonica 15x, Bismuthum metallicum 15x, Cadmium metallicum 15x, Calcarea fluorica 15x, Carbo vegetabilis 15x, Carduus marianus 15x Chelidonium majus 15x, Cinchona officinalis 15x, Cobaltum metallicum 15x, Cuprum metallicum 15x, Hydrofluoricum acidum 15x, Iris versicolor 15x, Manganum metallicum 15x, Mercurius vivus 15x, Niccolum metallicum 15x, Platinum metallicum 15x, Plumbum metallicum 15x, Stannum metallicum 15x, Thallium metallicum 15x, Beryllium metallicum 16x, Glycyrrhiza glabra 16x, Osmium metallicum 16x, Strontium carbonicum 16x, Titanium metallicum 16x.

Otc - Purpose Section

Formulated for associated symptoms such as fatigue, headaches, oversensitivity and sluggish elimination.

Inactive Ingredient Section

Inactive Ingredients: USP Purified Water; USP Gluten-free, non-GMO, organic cane alcohol 20%.

Questions Section

newtonlabs.net – Questions? 800.448.7256

Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30013

Warnings Section

WARNINGS: Keep out of reach of children. Do not use if tamper-evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding, ask a doctor before use.

Otc - Pregnancy Or Breast Feeding Section

If pregnant or breast-feeding, ask a doctor before use.

Otc - Keep Out Of Reach Of Children Section

Keep out of reach of children.

Package Label

Package Label (N061 L01)

Package Label (N061 L01)

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