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
LAXATIVES RUBILAX
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- LAXATIVES RUBILAX
- Generic name
- PSYLLIUM HUSKPOWDER
- Manufacturer
- Lydia Co., Ltd.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 87188d31-9fb1-5681-e053-2a91aa0a3022
- SPL ID
- 0ca8aa27-d06b-cbe4-e063-6394a90a629f
- Version
- 2
- Effective date
- 2023-12-16
- Source export date
- 2026-10-27
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/a758d73d4d838a965005e6adf01b928e2da86f99be0f8bbaeeb95f3b7acbe418/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 19:56:17
| Harmonized routes |
|---|
| ORAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| brand name | LAXATIVES RUBILAX | openfda.brand_name | |
| generic name | PSYLLIUM HUSKPOWDER | openfda.generic_name | |
| manufacturer name | Lydia Co., Ltd. | openfda.manufacturer_name | |
| ndc | package | 72988-0010-1 | openfda.package_ndc |
| ndc | package | 72988-0010-2 | openfda.package_ndc |
| ndc | product | 72988-0010 | openfda.product_ndc |
| ndc11 | package | 72988001002 | derived:openfda.package_ndc |
| ndc11 | package | 72988001001 | derived:openfda.package_ndc |
| spl id | 0ca8aa27-d06b-cbe4-e063-6394a90a629f | id | |
| spl set id | 87188d31-9fb1-5681-e053-2a91aa0a3022 | set_id | |
| unii | S8SJ19N2NX | openfda.unii | |
| unii | 0SHO53407G | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.