The following Structured Product Label (SPL) was submitted to the FDA by Marco Pharma International Llc. for the product Luffa (NDC 60986-2025). 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, dosage, 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.
Purging Luffa 6xHPUS
Goldenseal 4xHPUS
Cinnabaris 4xHPUS
Onion 6xHPUS
Salt 6xHPUS
Phosphorus 6xHPUS
Boneset 5xHPUS
Lungwort 2xHPUS
The letters HPUS indicates that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of United Sates.
For relief of sinus symptoms; hay-fever.
Adults take 1 tablet three times daily, dissolving on the tongue. For severe symptoms, take 1 tablet every hour until improvement is felt. Children receive 1/2 or less the adult amount.
If pregnant or breast-feeding, consult a health professional before use.
(Read Suggested Use Section)
In a Lactose base
Luffa.jpg
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