Guna-dermo Solution/ Drops
FDA Label NDC 17089-295

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-dermo (NDC 17089-295). 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

ARSENICUM ALBUM        6C    SKIN BLISTERS
BELLADONNA        6C    SWELLING
DULCAMARA        6C    MUSCLE SORENESS
ECHINACEA ANGUSTIFOLIA    6C    ANTI-INFECTION
GRAPHITES        6C    SKIN INFLAMMATION
INTERLEUKIN 1 BETA    7C    IMMUNE STRENGTHENING
INTERLEUKIN 2        4C    IMMUNE STRENGTHENING
MELATONIN        4C    HORMONAL SUPPORT
PLANTAGO MAJOR        4C    DETOXIFICATION
SULPHUR            6C    SENSITIVE SKIN

Uses

For the temporary relief of symptoms of general skin irritation and rashes such as: itching, dryness, hypersensitivity

Warnings

Stop use and ask doctor if symptoms of itching, dryness or hypersensitivity 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 and children 12 years and older    20 drops in a little water, 2 times per day
Children  between 12 years and 6 years of age    10 drops in a little water, 2 times per day
Children under 6 years     5 drops in a glass of water, 2 times per day

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