Aloe Socotrina

Aloe Socotrina is an FDA-registered drug product whose active ingredient is ALOE SOCOTRINA. It is labelled by Hahnemann Laboratories, INC. taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 37662-3536, label effective 20230706. It is one of 3 FDA drug label records sharing the active ingredient ALOE SOCOTRINA. 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 ALOE SOCOTRINA are most often described in connection with: indications condition, helps temporarily, relieve abdominal, discomfort digestive, irregularity intestinal. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

FDA lists 3 drug label records with ALOE SOCOTRINA as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

What is Aloe Socotrina used for?
The FDA label on file for this product does not include a full indications section. Other FDA labels sharing the active ingredient ALOE SOCOTRINA describe it in connection with: indications condition, helps temporarily, relieve abdominal, discomfort digestive, irregularity intestinal. Check the specific product label or ask a prescriber before use.

Who makes Aloe Socotrina?
Hahnemann Laboratories, INC. is the labeler of record for Aloe Socotrina. 3 FDA label records share the active ingredient ALOE SOCOTRINA, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does Aloe Socotrina 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 Aloe Socotrina 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.

Are there other products containing ALOE SOCOTRINA?
Yes. 3 FDA drug label records list ALOE SOCOTRINA as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has Aloe Socotrina 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.