warnings
WARNINGS: For external use only. Avoid contact with eyes, mucous membrane or broken skin.
RockSauce ICY COLD PAIN RELIEF
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
- RockSauce ICY COLD PAIN RELIEF
- Generic name
- MENTHOL
- Manufacturer
- Implus Footcare, LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- bd4fdff1-9174-31c2-e053-2a95a90a749f
- SPL ID
- 3239950d-8958-aaaa-e063-6394a90a8fa2
- Version
- 3
- Effective date
- 2025-04-07
- Source export date
- 2026-10-27
- Source partition
- 5
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/35717de05250cd386420cc8ede3b6010b48d18eea2af59afb0617fcabca634ec/drug-label-0005-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:05:07
| 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 | RockSauce ICY COLD PAIN RELIEF | openfda.brand_name | |
| generic name | MENTHOL | openfda.generic_name | |
| manufacturer name | Implus Footcare, LLC | openfda.manufacturer_name | |
| ndc | package | 81683-003-01 | openfda.package_ndc |
| ndc | product | 81683-003 | openfda.product_ndc |
| ndc11 | package | 81683000301 | derived:openfda.package_ndc |
| spl id | 3239950d-8958-aaaa-e063-6394a90a8fa2 | id | |
| spl set id | bd4fdff1-9174-31c2-e053-2a95a90a749f | 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.