warnings
Warnings Warnings: For external use only
Pharmacys Prescription Analgesic Gel
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
- Pharmacys Prescription Analgesic Gel
- Generic name
- MENTHOL
- Manufacturer
- American Consumer Products Corp
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 6f0725f2-833f-f3a0-e053-2a91aa0a3911
- SPL ID
- 2c69ab76-e3d1-1436-e063-6294a90aa515
- Version
- 4
- Effective date
- 2025-01-23
- Source export date
- 2026-09-28
- 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/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:18:17
| 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 | M012 | openfda.application_number | |
| brand name | Pharmacys Prescription Analgesic Gel | openfda.brand_name | |
| generic name | MENTHOL | openfda.generic_name | |
| manufacturer name | American Consumer Products Corp | openfda.manufacturer_name | |
| ndc | package | 72197-001-08 | openfda.package_ndc |
| ndc | product | 72197-001 | openfda.product_ndc |
| ndc11 | package | 72197000108 | derived:openfda.package_ndc |
| rxcui | 1039043 | openfda.rxcui | |
| spl id | 2c69ab76-e3d1-1436-e063-6294a90aa515 | id | |
| spl set id | 6f0725f2-833f-f3a0-e053-2a91aa0a3911 | 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.