Guna-tf Papilloma
FDA Label NDC 17089-281

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Guna Spa for the product Guna-tf Papilloma (NDC 17089-281). 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, uses, warnings, pregnancy, directions, questions, principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredients/Purpose

TRANSFER FACTOR HPV    7X    STIMULATES DEFENSIVE AND RECOVER FROM PAPILLOMA INFECTIONS

Uses


For the temporary relief of symptoms due to Papilloma infections such as: itching, burning, minor discomfort


Warnings

Stop use and ask doctor if symptoms of itching or minor discomfort worsen or persist more than 5 days

Keep this and all medicines out of reach of children

Pregnancy

If pregnant or breast-feeding ask a doctor before use

Directions

Take 15 minutes before meals
Adults 18 years and older    1 capsule per day with a little water

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