OKOUBAKA

OKOUBAKA AUBREVILLEI BARK ORAL HUMAN OTC DRUG

OKOUBAKA is an FDA drug label for the active ingredient OKOUBAKA AUBREVILLEI BARK manufactured by PEKANA Natuheilmittel GmbH 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 20221221.

Generic name
OKOUBAKA AUBREVILLEI BARK
Manufacturer
PEKANA Natuheilmittel GmbH
Product type
HUMAN OTC DRUG
Route
ORAL
Dosage form
N/A
NDC
59469-032
Application
N/A
Label effective
20221221

About this product

OKOUBAKA is an FDA-registered drug product whose active ingredient is OKOUBAKA AUBREVILLEI BARK. It is labelled by PEKANA Natuheilmittel GmbH taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 59469-032, label effective 20221221. 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 OKOUBAKA AUBREVILLEI BARK are most often described in connection with: relief occasional, diarrhea application, homeopathic remedy, designated usage, exclusively based, severe forms, disease clinically, proven therapy. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Ingredients: Okoubaka aubrevillei 2X Selected ingredients prepared by spagyric processes.

Indications & Usage

Indications For relief of occasional diarrhea. Application of this homeopathic remedy for the designated usage is exclusively based on homeopathic experience. With severe forms of this disease, a clinically proven therapy is indicated.

Dosage & Administration

Dosage Unless otherwise prescribed, adults take 15-20 drops, 3 times per day. For pediatric dosages, consult your practitioner.

Warnings

Warning If symptoms persist, contact a licensed practitioner. If you have known sensitivity to any of the ingredients, please consult your licensed practitioner before use. If you are pregnant or nursing a baby, seek the advice of a health care professional before use. Keep out of the reach of children. Protect from light and heat. Tamper Evident Do not use this product if tamper evident strip is broken or removed from base of cap.

Frequently asked questions

What is OKOUBAKA used for?
Indications For relief of occasional diarrhea. Application of this homeopathic remedy for the designated usage is exclusively based on homeopathic experience. With severe forms of this disease, a clinically proven therapy is indicated.

Who makes OKOUBAKA?
PEKANA Natuheilmittel GmbH is the labeler of record for OKOUBAKA.

What form does OKOUBAKA 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 OKOUBAKA 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 OKOUBAKA 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.