warnings
Warnings For rectal use only
Conlax
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
- Conlax
- Generic name
- BISACODYL
- Manufacturer
- Bliss GVS Pharma Limited
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 7d25990b-6f7c-1eac-e053-2a91aa0a7022
- SPL ID
- 29c2887d-d165-e58b-e063-6394a90a62b8
- Version
- 5
- Effective date
- 2024-12-21
- Source export date
- 2026-09-28
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:15:52
| 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 | Conlax | openfda.brand_name | |
| generic name | BISACODYL | openfda.generic_name | |
| manufacturer name | Bliss GVS Pharma Limited | openfda.manufacturer_name | |
| ndc | package | 72701-102-05 | openfda.package_ndc |
| ndc | package | 72701-102-30 | openfda.package_ndc |
| ndc | package | 72701-102-12 | openfda.package_ndc |
| ndc | package | 72701-102-08 | openfda.package_ndc |
| ndc | package | 72701-102-10 | openfda.package_ndc |
| ndc | package | 72701-102-28 | openfda.package_ndc |
| ndc | package | 72701-102-16 | openfda.package_ndc |
| ndc | package | 72701-102-04 | openfda.package_ndc |
| ndc | product | 72701-102 | openfda.product_ndc |
| ndc11 | package | 72701010210 | derived:openfda.package_ndc |
| ndc11 | package | 72701010216 | derived:openfda.package_ndc |
| ndc11 | package | 72701010205 | derived:openfda.package_ndc |
| ndc11 | package | 72701010208 | derived:openfda.package_ndc |
| ndc11 | package | 72701010204 | derived:openfda.package_ndc |
| ndc11 | package | 72701010228 | derived:openfda.package_ndc |
| ndc11 | package | 72701010230 | derived:openfda.package_ndc |
| ndc11 | package | 72701010212 | derived:openfda.package_ndc |
| rxcui | 198509 | openfda.rxcui | |
| spl id | 29c2887d-d165-e58b-e063-6394a90a62b8 | id | |
| spl set id | 7d25990b-6f7c-1eac-e053-2a91aa0a7022 | 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.