FREEZE IT Menthol
- Product NDC
- 71726-004
- 11-digit product format
- 717260004
- Labeler code
- 71726
- Product ID
- 71726-004_6e80d075-fdc1-448f-9e11-7a6980359ef7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Menthol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- LiquidCapsule Manufacturing LLC
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-06-05
- Substance
- MENTHOL
- Active strength
- 3.5 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71726-004-02 | 71726000402 | 113.4 g in 1 TUBE (71726-004-02) | 113.4 g | 2025-06-05 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| FREEZE IT Menthol 3.5% Gel | LiquidCapsule Manufacturing LLC | 2025-06-05 | HUMAN OTC DRUG LABEL | 1 |