warnings
STOP USE AND ASK DOCTOR If symptoms worsen or persist for more than 7 days, or if pregnant or nursing, consult a licensed practitioner.
Camphora
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
- Camphora
- Generic name
- CAMPHOR (NATURAL)
- Manufacturer
- Washington Homeopathic Products
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 0876d0ba-0e05-61c5-e063-6294a90aba7e
- SPL ID
- 2cc87194-4c97-f4af-e063-6294a90a596b
- Version
- 2
- Effective date
- 2025-01-28
- Source export date
- 2026-10-12
- Source partition
- 13
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 03:09:38
| 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 | Camphora | openfda.brand_name | |
| generic name | CAMPHOR (NATURAL) | openfda.generic_name | |
| manufacturer name | Washington Homeopathic Products | openfda.manufacturer_name | |
| ndc | package | 71919-811-05 | openfda.package_ndc |
| ndc | product | 71919-811 | openfda.product_ndc |
| ndc11 | package | 71919081105 | derived:openfda.package_ndc |
| spl id | 2cc87194-4c97-f4af-e063-6294a90a596b | id | |
| spl set id | 0876d0ba-0e05-61c5-e063-6294a90aba7e | set_id | |
| unii | N20HL7Q941 | 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.