warnings
Warnings For external use only avoid contact with eyes and mucous membranes
China-Gel Topical Pain Reliever
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
- China-Gel Topical Pain Reliever
- Generic name
- MENTHOL AND CAMOHOR (SYNTHETIC)
- Manufacturer
- China-Gel, LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 254abae9-ef1b-5a90-e054-00144ff88e88
- SPL ID
- 42c8b69f-5f4d-a88b-e063-6294a90a6eae
- Version
- 7
- Effective date
- 2025-11-04
- Source export date
- 2026-09-28
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:26:33
| Harmonized routes |
|---|
| TOPICAL |
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 | China-Gel Topical Pain Reliever | openfda.brand_name | |
| generic name | MENTHOL AND CAMOHOR (SYNTHETIC) | openfda.generic_name | |
| manufacturer name | China-Gel, LLC | openfda.manufacturer_name | |
| ndc | package | 76305-301-02 | openfda.package_ndc |
| ndc | package | 76305-301-06 | openfda.package_ndc |
| ndc | package | 76305-301-07 | openfda.package_ndc |
| ndc | package | 76305-301-03 | openfda.package_ndc |
| ndc | package | 76305-301-05 | openfda.package_ndc |
| ndc | package | 76305-301-13 | openfda.package_ndc |
| ndc | package | 76305-301-04 | openfda.package_ndc |
| ndc | product | 76305-301 | openfda.product_ndc |
| ndc11 | package | 76305030103 | derived:openfda.package_ndc |
| ndc11 | package | 76305030102 | derived:openfda.package_ndc |
| ndc11 | package | 76305030105 | derived:openfda.package_ndc |
| ndc11 | package | 76305030104 | derived:openfda.package_ndc |
| ndc11 | package | 76305030113 | derived:openfda.package_ndc |
| ndc11 | package | 76305030106 | derived:openfda.package_ndc |
| ndc11 | package | 76305030107 | derived:openfda.package_ndc |
| rxcui | 1312283 | openfda.rxcui | |
| rxcui | 1722364 | openfda.rxcui | |
| spl id | 42c8b69f-5f4d-a88b-e063-6294a90a6eae | id | |
| spl set id | 254abae9-ef1b-5a90-e054-00144ff88e88 | 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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.