GUNA-IL 12
GUNA-IL 12 is an FDA drug label for the active ingredient INTERLEUKIN-12 HUMAN RECOMBINANT 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 20260611.
- Generic name
- INTERLEUKIN-12 HUMAN RECOMBINANT
- Manufacturer
- Guna spa
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 17089-390
- Application
- N/A
- Label effective
- 20260611
About this product
GUNA-IL 12 is an FDA-registered drug product whose active ingredient is INTERLEUKIN-12 HUMAN RECOMBINANT. It is labelled by Guna spa taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 17089-390, label effective 20260611. 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 INTERLEUKIN-12 HUMAN RECOMBINANT 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
DIRECTIONS Take 15 minutes before meals. Adults and children 12 years and older 20 drops twice a day in a little water. Hold in the mouth for about 30 seconds then swallow. Children between 12 years and 6 years of age 10 drops twice a day in a little water. Hold in the mouth for about 30 seconds then swallow. Children under 6 years consult a physician.
Warnings
WARNINGS Stop use and ask doctor if symptoms worsen or persist more than 3 days
Frequently asked questions
What is GUNA-IL 12 used for?
Take 15 minutes before meals.
Who makes GUNA-IL 12?
Guna spa is the labeler of record for GUNA-IL 12.
What form does GUNA-IL 12 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-IL 12 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-IL 12 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.