PROALLER

PROALLER is an FDA-registered drug product whose active ingredient is AILANTHUS ALTISSIMA WHOLE, OKOUBAKA AUBREVILLEI BARK, EUPHRASIA STRICTA, GRATIOLA OFFICINALIS, JUGLANS REGIA WHOLE, SMILAX REGELII ROOT, AND TARAXACUM OFFICINALE WHOLE. It is labelled by PEKANA Naturheilmittel taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 59469-116, label effective 20221219. 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.

Across FDA labelling, products containing AILANTHUS ALTISSIMA WHOLE, OKOUBAKA AUBREVILLEI BARK, EUPHRASIA STRICTA, GRATIOLA OFFICINALIS, JUGLANS REGIA WHOLE, SMILAX REGELII ROOT, AND TARAXACUM OFFICINALE WHOLE are most often described in connection with: temporary relief, hay fever, symptoms application, homeopathic remedy, designated usage, exclusively based, severe forms, disease clinically. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Indications For temporary relief of allergies and hay fever symptoms. 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 Unless otherwise prescribed, adults take 15-20 drops, 3 times per day. For pediatric dosages, consult your practitioner.

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.

What is PROALLER used for?
Indications For temporary relief of allergies and hay fever symptoms. 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 PROALLER?
PEKANA Naturheilmittel is the labeler of record for PROALLER.

What form does PROALLER 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 PROALLER 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 PROALLER 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.