warnings
Warnings For rectal use only.
Meijer Gentle Laxative
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
- Meijer Gentle Laxative
- Generic name
- BISACODYL
- Manufacturer
- Meijer Distribution Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- b49786a1-f0b9-45ae-b8f6-683489c54e76
- SPL ID
- a34ed0dd-d1c1-480e-9f9c-f703d0da0230
- Version
- 6
- Effective date
- 2024-12-18
- Source export date
- 2026-10-12
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:52:59
| Harmonized routes |
|---|
| RECTAL |
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 |
|---|---|---|---|
| application number | M007 | openfda.application_number | |
| brand name | Meijer Gentle Laxative | openfda.brand_name | |
| generic name | BISACODYL | openfda.generic_name | |
| manufacturer name | Meijer Distribution Inc. | openfda.manufacturer_name | |
| ndc | package | 41250-665-04 | openfda.package_ndc |
| ndc | product | 41250-665 | openfda.product_ndc |
| ndc11 | package | 41250066504 | derived:openfda.package_ndc |
| rxcui | 198509 | openfda.rxcui | |
| spl id | a34ed0dd-d1c1-480e-9f9c-f703d0da0230 | id | |
| spl set id | b49786a1-f0b9-45ae-b8f6-683489c54e76 | set_id | |
| unii | 10X0709Y6I | 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.