warnings
Warnings For external use only Allergy alert: This product contains natural rubber latex which may cause allergic reactions
EXTRA STRENGTH HUA TUO PAIN RELIEVING
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 RELIEVING
- Generic name
- CAMPHOR AND MENTHOL
- Manufacturer
- Zhejiang Dingtai Pharmaceutical Co., Ltd
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 9850754b-ac94-4ec6-b75a-8096e5ac9456
- SPL ID
- 4345be21-4ba4-122d-e063-6394a90a5fa7
- Version
- 5
- Effective date
- 2025-11-10
- Source export date
- 2026-09-28
- 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/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:38:09
| 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 RELIEVING | openfda.brand_name | |
| generic name | CAMPHOR AND MENTHOL | openfda.generic_name | |
| manufacturer name | Zhejiang Dingtai Pharmaceutical Co., Ltd | openfda.manufacturer_name | |
| ndc | package | 69070-307-01 | openfda.package_ndc |
| ndc | product | 69070-307 | openfda.product_ndc |
| ndc11 | package | 69070030701 | derived:openfda.package_ndc |
| rxcui | 2118540 | openfda.rxcui | |
| spl id | 4345be21-4ba4-122d-e063-6394a90a5fa7 | id | |
| spl set id | 9850754b-ac94-4ec6-b75a-8096e5ac9456 | 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.