Arctic Ice Pain Relieving Gel
- Product NDC
- 87510-006
- 11-digit product format
- 875100006
- Labeler code
- 87510
- Product ID
- 87510-006_5cb85b44-bc75-ea03-e063-6294a90a16c6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Menthol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- ONEST LIMITED
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-08-15
- Marketing end
- 2027-10-01
- Substance
- MENTHOL
- Active strength
- 1.25 g/100g
- NDC exclude flag
- No
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Arctic Ice Pain Relieving Gel
Active Ingredients#
| Ingredient | Strength |
|---|---|
| MENTHOL | 1.25 g/100g |
openFDA label cross-check#
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.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 87510-006-01 | 87510000601 | 198 g in 1 JAR (87510-006-01) | 198 g | 2026-08-15 | 2027-10-01 | No | No | Historical |