warnings
Warnings For external use only Allergy alert: This product contains natural rubber latex which may cause allergic reactions.
EXTRA STRENGTH HUA TUO PAIN 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
- EXTRA STRENGTH HUA TUO PAIN RELIEF
- Generic name
- CAMPHOR AND MENTHOL
- Manufacturer
- MADISON ONE ACME INC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 0f269a41-4b56-4e22-b9cb-17d99bf76a57
- SPL ID
- 4346c26f-c1e0-1ac9-e063-6394a90a6a70
- Version
- 3
- Effective date
- 2025-11-10
- Source export date
- 2026-11-06
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/97001096994db9ca8cee114e6c3bb5298d3c573158ffc1ab8692d82e76a3eb40/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 06:55:21
| Harmonized routes |
|---|
| TRANSDERMAL |
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 |
|---|---|---|---|
| application number | M017 | openfda.application_number | |
| brand name | EXTRA STRENGTH HUA TUO PAIN RELIEF | openfda.brand_name | |
| generic name | CAMPHOR AND MENTHOL | openfda.generic_name | |
| manufacturer name | MADISON ONE ACME INC | openfda.manufacturer_name | |
| ndc | package | 55614-630-01 | openfda.package_ndc |
| ndc | product | 55614-630 | openfda.product_ndc |
| ndc11 | package | 55614063001 | derived:openfda.package_ndc |
| rxcui | 2118540 | openfda.rxcui | |
| spl id | 4346c26f-c1e0-1ac9-e063-6394a90a6a70 | id | |
| spl set id | 0f269a41-4b56-4e22-b9cb-17d99bf76a57 | set_id | |
| unii | L7T10EIP3A | openfda.unii | |
| unii | 5TJD82A1ET | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
Report any unexpected side effects from the use of this product to the FDA MedWatch Program.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.