Natrum sulphuricum

Natrum sulphuricum is an FDA-registered drug product whose active ingredient is SODIUM SULFATE. It is labelled by Boiron taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 0220-3635, label effective 20231114. It is one of 12 FDA drug label records sharing the active ingredient SODIUM SULFATE. 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 SODIUM SULFATE are most often described in connection with: bronchial irritation, worsened humidity. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Bronchial irritation worsened by humidity*

Adults and children: At the onset of symptoms, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.

FDA lists 12 drug label records with SODIUM SULFATE 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.

2 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.

What is Natrum sulphuricum used for?
Bronchial irritation worsened by humidity*

Who makes Natrum sulphuricum?
Boiron is the labeler of record for Natrum sulphuricum. 12 FDA label records share the active ingredient SODIUM SULFATE, 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 Natrum sulphuricum 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 Natrum sulphuricum 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 SODIUM SULFATE?
Yes. 12 FDA drug label records list SODIUM SULFATE 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 Natrum sulphuricum been recalled?
2 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.

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.