Sovereign Silver Gel
FDA Label NDC 52166-015

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Natural Immunogenics Corp.dba Sovereign Naturals for the product Sovereign Silver (NDC 52166-015). 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, warnings, otc - ask doctor, dosage & administration, indications & usage, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

Ingredients

ACTIVE:  Argentum Metallicum 10x, 20x and 30x HPUS

Inactive Ingredient

INACTIVE

Silver hydrosol, carbopol and sodium hydroxide

Otc - Purpose

Purpose

Natural healing gel skin care

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Warnings

Warnings

For external use only. Ask a doctor before use if you have deep or puncture wounds, animal bites or serious burns.

Otc - Ask Doctor

Stop and ask a doctor if symptoms persist or worsen after 3 days of use. Do not use if seal is broken

Dosage & Administration

Directions

Gently clean affected area. Apply a liberal, consistent layer of Skin Care Gel over affected area. Repeat 3 times per day or as often as needed to relieve symptoms. Safe on sensitive skin.

Indications & Usage

Indications for Use

For relief of symptoms due to skin eruptions from acne, eczema, minor infection, rashes, blisters -Sunburn – Razor Burn – minor nicks & cuts – redness – minor inflammation

Product Label

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