warnings
Warnings For external use only.
Topical Analgesic
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
- Topical Analgesic
- Generic name
- MENTHOL
- Manufacturer
- Youngevity International Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- b4693947-f5b3-6fd3-e053-2995a90ab581
- SPL ID
- 41ca9fa1-0b43-425a-e063-6394a90afac0
- Version
- 7
- Effective date
- 2025-10-22
- Source export date
- 2026-11-06
- 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/2026-11-06/b00a73f24c6ff050408c570063640e3d80d1f71dfc9a165d1cf072a25659445a/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 07:02:51
| 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 | Topical Analgesic | openfda.brand_name | |
| generic name | MENTHOL | openfda.generic_name | |
| manufacturer name | Youngevity International Inc. | openfda.manufacturer_name | |
| ndc | package | 80986-101-01 | openfda.package_ndc |
| ndc | product | 80986-101 | openfda.product_ndc |
| ndc11 | package | 80986010101 | derived:openfda.package_ndc |
| rxcui | 2391332 | openfda.rxcui | |
| spl id | 41ca9fa1-0b43-425a-e063-6394a90afac0 | id | |
| spl set id | b4693947-f5b3-6fd3-e053-2995a90ab581 | set_id | |
| unii | L7T10EIP3A | 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.