warnings
Warnings: For external use only
Pain Relieving Roll-On
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
- Pain Relieving Roll-On
- Generic name
- MENTHOL, CAMPHOR, CAPSAICIN
- Manufacturer
- AHC VENTURES CORP DBA CRY
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 799751f3-726a-42de-934e-dbc3cd1cb8b8
- SPL ID
- 3dd5fc5a-32c4-78bf-e063-6394a90af02a
- Version
- 4
- Effective date
- 2025-09-02
- Source export date
- 2026-10-27
- Source partition
- 14
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/9122bd1bdced046e8f62ea012d80757473b7d83ea1faeea61faef490e06fd630/drug-label-0014-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 21:10:02
| 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 | Pain Relieving Roll-On | openfda.brand_name | |
| generic name | MENTHOL, CAMPHOR, CAPSAICIN | openfda.generic_name | |
| manufacturer name | AHC VENTURES CORP DBA CRY | openfda.manufacturer_name | |
| ndc | package | 68678-040-90 | openfda.package_ndc |
| ndc | product | 68678-040 | openfda.product_ndc |
| ndc11 | package | 68678004090 | derived:openfda.package_ndc |
| spl id | 3dd5fc5a-32c4-78bf-e063-6394a90af02a | id | |
| spl set id | 799751f3-726a-42de-934e-dbc3cd1cb8b8 | set_id | |
| unii | S07O44R1ZM | openfda.unii | |
| 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.