ARCTIC ICE
- Product NDC
- 76176-206
- 11-digit product format
- 761760206
- Labeler code
- 76176
- Product ID
- 76176-206_5b309e25-ab1f-de41-e063-6294a90a3839
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD.
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-10-01
- Substance
- MENTHOL
- Active strength
- 1.25 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- 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
- Listing expiration
- 2027-12-31
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 | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 76176-206-01 | 76176020601 | 198 g in 1 JAR (76176-206-01) | 198 g | 2023-10-01 | No | No | Current |