Dosage and administration
Adults and children 3 years of age and older: Apply to the affected area not more than 3 to 4 times daily. • Children under 3 years of age: Consult a doctor.
Adults and children 3 years of age and older: Apply to the affected area not more than 3 to 4 times daily. • Children under 3 years of age: Consult a doctor.
camphor 3.5%
capsaicin 0.18%
menthol 1.25%
methyl salicylate 12%
pain relieving gel
For the temporary relief of minor aches and pains of muscles and joints
For external use only.
Do not use otherwise than as directed.
When using this product • avoid contact with the eyes and mucous membranes
Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days. Discontinue use if excessive irritation of the skin develops
Keep out of reach of chilren. If swallowed, get medical help or contact a Poison Control Center right away.
Aloe vera extract, carbomer 940, eucalyptus globulus leaf essential oil, glycerin, guaiacum, paullinia cupana fruit powder, phenoxyethanol, rosmarinus officinalis (rosemary) leaf oil, rosmarinus officinalis (rosemary) leaf powder, sodium acrylate/sodium acryloyldimethyltaurate copolymer (4000000 MW), triethanolamine, water.
KASEHA
Pain Relieving Gel
2 fl oz (60mL)
DISTRIBUTED BY:
DENALI NATURAL PRODUCTS,
1411 N. BATAVIA ST STE 116
ORANGE, CA 92867
MADE IN MEXICO
TEL. 562-390-2873
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 83056-002-02 | 2025-08-01 | C162847 | 48780-1 | 3b156c62-303a-fb37-e063-e6dba90a4e07 | KASEHA Pain relieving gel gold |
| 83056-002-02 | 2025-07-29 | C162847 | 48780-1 | 3b156c62-303a-fb37-e063-e6dba90a4e07 | KASEHA Pain relieving gel gold |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 83056-002 | 83056-002-02 |
Every source-derived ingredient row is available through these pages.
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 3b03087a-159a-8697-e063-6294a90a195f | fbc27909-8df4-5d99-e053-6294a90a373e | 2025-07-28 | Warnings | fbc27909-8df4-5d99-e053-6294a90a373e |
Adverse event summaries are temporarily unavailable. Other product information remains available.