warnings
Warnings For external use only
EXTREME EMU
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
- EXTREME EMU
- Generic name
- MENTHOL, METHYL SALICYLATE
- Manufacturer
- Renu Laboratories, LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 4393b57b-1e70-b8dd-e063-6294a90ae748
- SPL ID
- 4393a4f8-c1e1-3430-e063-6294a90a3933
- Version
- 1
- Effective date
- 2025-11-14
- Source export date
- 2026-09-28
- 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/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:40:56
| 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 | EXTREME EMU | openfda.brand_name | |
| generic name | MENTHOL, METHYL SALICYLATE | openfda.generic_name | |
| manufacturer name | Renu Laboratories, LLC | openfda.manufacturer_name | |
| ndc | package | 76348-495-04 | openfda.package_ndc |
| ndc | product | 76348-495 | openfda.product_ndc |
| ndc11 | package | 76348049504 | derived:openfda.package_ndc |
| rxcui | 311503 | openfda.rxcui | |
| spl id | 4393a4f8-c1e1-3430-e063-6294a90a3933 | id | |
| spl set id | 4393b57b-1e70-b8dd-e063-6294a90ae748 | set_id | |
| unii | L7T10EIP3A | openfda.unii | |
| unii | LAV5U5022Y | 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.