GUNA-SLEEP
GUNA-SLEEP is an FDA drug label for the active ingredient AVENA SATIVA FLOWERING TOP - CANAKINUMAB - CHAMOMILE - HELLEBORUS NIGER ROOT - MELATONIN - MELISSA OFFICINALIS - PULSATILLA VULGARIS - SEROTONIN - STRYCHNOS IGNATII SEED - SUS SCROFA PINEAL GLAND - VALERIAN - manufactured by Guna spa administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260610.
- Generic name
- AVENA SATIVA FLOWERING TOP - CANAKINUMAB - CHAMOMILE - HELLEBORUS NIGER ROOT - MELATONIN - MELISSA OFFICINALIS - PULSATILLA VULGARIS - SEROTONIN - STRYCHNOS IGNATII SEED - SUS SCROFA PINEAL GLAND - VALERIAN -
- Manufacturer
- Guna spa
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 17089-294
- Application
- N/A
- Label effective
- 20260610
About this product
GUNA-SLEEP is an FDA-registered drug product whose active ingredient is AVENA SATIVA FLOWERING TOP - CANAKINUMAB - CHAMOMILE - HELLEBORUS NIGER ROOT - MELATONIN - MELISSA OFFICINALIS - PULSATILLA VULGARIS - SEROTONIN - STRYCHNOS IGNATII SEED - SUS SCROFA PINEAL GLAND - VALERIAN -. It is labelled by Guna spa taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 17089-294, label effective 20260610. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.
What it is used for
Across FDA labelling, products containing AVENA SATIVA FLOWERING TOP - CANAKINUMAB - CHAMOMILE - HELLEBORUS NIGER ROOT - MELATONIN - MELISSA OFFICINALIS - PULSATILLA VULGARIS - SEROTONIN - STRYCHNOS IGNATII SEED - SUS SCROFA PINEAL GLAND - VALERIAN - are most often described in connection with: take minutes. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Take 15 minutes before meals.
Dosage & Administration
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: consult a physician
Warnings
Stop use and ask doctor if symptoms persist more than 5 days. If pregnant or breast-feeding ask a health professional before use. Keep out of reach of children . In case of overdose, get medical help or contact a Poison Control Center right away. Contains ethyl alcohol 30%
Frequently asked questions
What is GUNA-SLEEP used for?
Take 15 minutes before meals.
Who makes GUNA-SLEEP?
Guna spa is the labeler of record for GUNA-SLEEP.
What form does GUNA-SLEEP come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is GUNA-SLEEP prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Has GUNA-SLEEP been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.
Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.