warnings
WARNINGS SECTION Warning : Consult a doctor if symptoms persist more than 3 days or worsen. If pregnant or nursing , ask a doctor before use. Keep out of reach of children. Do not use if tamper-evident band is missing or broken.
Belladonna
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
- Belladonna
- Generic name
- BELLADONNA
- Manufacturer
- Historical Remedies
- Product type
- HUMAN OTC DRUG
- SPL set ID
- c6784560-5d61-78b3-e053-2995a90adc25
- SPL ID
- 4093c268-5be2-b0b5-e063-6394a90a66f1
- Version
- 9
- Effective date
- 2025-10-07
- 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 02:54:23
| 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 | Belladonna | openfda.brand_name | |
| generic name | BELLADONNA | openfda.generic_name | |
| manufacturer name | Historical Remedies | openfda.manufacturer_name | |
| ndc | package | 57556-012-02 | openfda.package_ndc |
| ndc | product | 57556-012 | openfda.product_ndc |
| ndc11 | package | 57556001202 | derived:openfda.package_ndc |
| spl id | 4093c268-5be2-b0b5-e063-6394a90a66f1 | id | |
| spl set id | c6784560-5d61-78b3-e053-2995a90adc25 | set_id | |
| unii | WQZ3G9PF0H | 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.