Guna-spasm Solution/ Drops
FDA Label NDC 17089-348

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-spasm (NDC 17089-348). 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.

Label Section Quick Index

Active Ingredients/Purpose

AGARICUS CAMPESTRIS         4X    ANTISPASTIC
ANTI INTERLEUKIN 1 ALPHA      4C    ANTI-INFLAMMATORY
ATROPINUM SULFURICUM         6X    PAIN RELIEF
BERBERIS VULGARIS         3X    DETOXIFICATION
BETA-ENDORPHIN             4C    PAIN RELIEF
CHELIDONIUM MAJUS         4X    DETOXIFICATION
COBALTUM METALLICUM         4X    ANTISPASTIC
COLOCYNTHIS             4X    BACK SORE
GELSEMIUM              6X     ANALGESIC
INTERLEUKIN 10             4C    ANTI-INFLAMMATORY
MAGNESIUM METALLICUM         4X    ANTISPASTIC
MELATONIN             4C    ANTISPASTIC
SYMPATHETIC NERVE        200X    PAIN RELIEF
VAGAL NERVE            6X    PAIN RELIEF

Uses

For the temporary relief of symptoms of minor musculoskeletal pain due to Spasm and Hypertonic Muscles

Warnings

Stop use and ask doctor if symptoms of spasms 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, 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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