warnings
Warnings: If symptoms persist or worsen, or if pregnant or nursing, consult a doctor.
Constipation Relief
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
- Constipation Relief
- Generic name
- ALUMINUM OXIDE, BRYONIA ALBA ROOT, SODIUM CHLORIDE, GRAPHITE, SILICON DIOXIDE
- Manufacturer
- Homeocare Laboratories
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 62374240-cd14-44e2-9405-5f8996faf047
- SPL ID
- 4836c0cb-504d-e24b-e063-6294a90a4e31
- Version
- 3
- Effective date
- 2026-01-12
- Source export date
- 2026-09-28
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:07:15
| Harmonized routes |
|---|
| SUBLINGUAL |
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 | Constipation Relief | openfda.brand_name | |
| generic name | ALUMINUM OXIDE, BRYONIA ALBA ROOT, SODIUM CHLORIDE, GRAPHITE, SILICON DIOXIDE | openfda.generic_name | |
| manufacturer name | Homeocare Laboratories | openfda.manufacturer_name | |
| ndc | package | 61727-304-21 | openfda.package_ndc |
| ndc | product | 61727-304 | openfda.product_ndc |
| ndc11 | package | 61727030421 | derived:openfda.package_ndc |
| spl id | 4836c0cb-504d-e24b-e063-6294a90a4e31 | id | |
| spl set id | 62374240-cd14-44e2-9405-5f8996faf047 | set_id | |
| unii | LMI26O6933 | openfda.unii | |
| unii | 4QQN74LH4O | openfda.unii | |
| unii | ETJ7Z6XBU4 | openfda.unii | |
| unii | 451W47IQ8X | openfda.unii | |
| unii | T7J046YI2B | 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.