Solidago Liquid
FDA Label NDC 60986-1020

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Marco Pharma International Llc. for the product Solidago (NDC 60986-1020). 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 active ingredients, purpose, otc - keep out of reach of children, suggested use, warnings, dosage & administration, inactive ingredients, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredients

Goldenrod 1x HPUS

Bearberry 1x HPUS

Pareira brava 3x HPUS

Saw Palmetto 1x HPUS

Aspen 2x HPUS

Stavesacre 3x HPUS

Spanish Fly 4x HPUS

Terpentine 6x HPUS

Sodium borate 8x HPUS

The letters HPUS indicates that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of United Sates.

Purpose

For discomfort during urination and lower back pain in the kidney region.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Suggested Use

Adults: Take 40 drops in tepid water three times daily. For severe symptoms, take 40 drops four to five time daily. After improvement is felt, take 40 drops three times daily. Children receive 1/2 or less of the adult amount.

Warnings

If pregnant or breast-feeding, consult a health professional before use.

Dosage & Administration

(Read Suggested Use Section)

Inactive Ingredients

Ethyl Alcohol (54% by vol.) and Water

Package Label.Principal Display Panel

Solidago.jpg

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