warnings
Warnings: If symptoms persist or worsen, or if pregnant or nursing, consult a doctor. Keep out of reach of children. Do not use if cap seal is broken or missing.
Blatrol Bladder 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
- Blatrol Bladder Relief
- Generic name
- LYTTA VESICATORIA, CAUSTICUM, EQUISETUM HYEMALE, CHONDRODENDRON TOMENTOSUM ROOT, SAW PALMETTO, SEPIA OFFICINALIS JUICE, DELPHINIUM STAPHISAGRIA SEED
- Manufacturer
- Homeocare Laboratories
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 1c26c0b6-6623-417f-8317-eaeb923045e9
- SPL ID
- 7e58d849-dada-b924-e053-2991aa0aef01
- Version
- 2
- Effective date
- 2018-12-31
- Source export date
- 2026-10-27
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/be847f9aea8d80a2cb7e9771acd1143be084664192ecf8f5be8ac1024116f4f0/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:15:34
| 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 | Blatrol Bladder Relief | openfda.brand_name | |
| generic name | LYTTA VESICATORIA, CAUSTICUM, EQUISETUM HYEMALE, CHONDRODENDRON TOMENTOSUM ROOT, SAW PALMETTO, SEPIA OFFICINALIS JUICE, DELPHINIUM STAPHISAGRIA SEED | openfda.generic_name | |
| manufacturer name | Homeocare Laboratories | openfda.manufacturer_name | |
| ndc | package | 61727-318-21 | openfda.package_ndc |
| ndc | product | 61727-318 | openfda.product_ndc |
| ndc11 | package | 61727031821 | derived:openfda.package_ndc |
| spl id | 7e58d849-dada-b924-e053-2991aa0aef01 | id | |
| spl set id | 1c26c0b6-6623-417f-8317-eaeb923045e9 | set_id | |
| unii | 395A3P448Z | openfda.unii | |
| unii | J7WWH9M8QS | openfda.unii | |
| unii | DD5FO1WKFU | openfda.unii | |
| unii | 00543AP1JV | openfda.unii | |
| unii | QDL83WN8C2 | openfda.unii | |
| unii | 3Q034RO3BT | openfda.unii | |
| unii | 59677RXH25 | 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.