LAXATIVES RUBILAX
LAXATIVES RUBILAX is an FDA drug label for the active ingredient PSYLLIUM HUSKPOWDER manufactured by Lydia Co., Ltd. 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 20231216.
- Generic name
- PSYLLIUM HUSKPOWDER
- Manufacturer
- Lydia Co., Ltd.
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 72988-0010
- Application
- N/A
- Label effective
- 20231216
About this product
LAXATIVES RUBILAX is an FDA-registered drug product whose active ingredient is PSYLLIUM HUSKPOWDER. It is labelled by Lydia Co., Ltd. taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 72988-0010, label effective 20231216. 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 PSYLLIUM HUSKPOWDER are most often described in connection with: adults take, twice day, evening empty, stomach however, minimum amount, first time, gradually increases. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
adults take intake does of 3.5g twice a day morning and evening on an empty stomach, however, taking the minimum amount of the first time and watching the shape and condition of the stomach gradually increases or decreases
Dosage & Administration
for oral use only
Warnings
do not administer to the following patients, the product contains lactose, patients with rare hereditary problems of galactose intolerance, the lapp deficiency or glucose-galactose malabsorption should not take this medicine
Frequently asked questions
What is LAXATIVES RUBILAX used for?
adults take intake does of 3.5g twice a day morning and evening on an empty stomach, however, taking the minimum amount of the first time and watching the shape and condition of the stomach gradually increases or decreases
Who makes LAXATIVES RUBILAX?
Lydia Co., Ltd. is the labeler of record for LAXATIVES RUBILAX.
What form does LAXATIVES RUBILAX 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 LAXATIVES RUBILAX 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 LAXATIVES RUBILAX 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.