Guna-pms Solution/ Drops
FDA Label NDC 17089-290

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-pms (NDC 17089-290). 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, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredients/Purpose

ARSENICUM ALBUM    6C    MOOD SUPPORT
BETA-ESTRADIOL    6X    FOR  VAGINAL DRYNESS
CHAMOMILLA    6C    CALMING
HYDRASTIS CANADENSIS    6C    ANALGESIC
HYPOPHYSIS    8X    HORMONAL REGULATION
LACHESIS MUTUS    4C    ANXIETY
MAGNESIA PHOSPHORICA    6C    METABOLIC SUPPORT
MELATONIN    4C    HORMONAL BALANCE
NUX VOMICA    6C    MOOD SUPPORT
OOPHORINUM    8X    FOR IRREGULAR MENSES
PROGESTERONE    6X    FOR IRREGULAR MENSES
SULFUR        6C    DETOXIFICATION

Uses

For the temporary relief of symptoms due to Premenstrual Syndrome such as: moodiness, cramping, backache

Warnings

Stop use and ask doctor if symptoms of moodiness, cramping or backache do not improve, 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 under 12 years Ask a physician

* Please review the disclaimer below.