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
- 2026-10-12
- 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/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:31:45
| 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.