warnings
WARNINGS In case of overdose, get medical help or contact a poison control center right away. Keep out of the reach of children. If pregnant or breastfeeding, ask a healthcare professional before use.
Pulsatilla 7131
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
- Pulsatilla 7131
- Generic name
- PULSATILLA
- Manufacturer
- Professional Complementary Health Formulas
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 02df74e5-dcb0-4942-8c07-87faf18f145d
- SPL ID
- 336fa763-4c54-4dba-a649-023c0606e5ea
- Version
- 2
- Effective date
- 2026-01-08
- Source export date
- 2026-10-12
- 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/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:02:57
| 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 | Pulsatilla 7131 | openfda.brand_name | |
| generic name | PULSATILLA | openfda.generic_name | |
| manufacturer name | Professional Complementary Health Formulas | openfda.manufacturer_name | |
| ndc | package | 63083-7131-1 | openfda.package_ndc |
| ndc | product | 63083-7131 | openfda.product_ndc |
| ndc11 | package | 63083713101 | derived:openfda.package_ndc |
| spl id | 336fa763-4c54-4dba-a649-023c0606e5ea | id | |
| spl set id | 02df74e5-dcb0-4942-8c07-87faf18f145d | set_id | |
| unii | 24K790T39B | 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.