2.5% Menthol PAIN RELIEF
- Product NDC
- 52000-440
- 11-digit product format
- 520000440
- Labeler code
- 52000
- Product ID
- 52000-440_8b302a49-b577-429b-b508-b386e56c2af3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Menthol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Universal Distribution Center LLC
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-01-19
- Substance
- MENTHOL, UNSPECIFIED FORM
- Active strength
- 25 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- 2.5% Menthol PAIN RELIEF
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL, UNSPECIFIED FORM | 25 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
| Rxcui | 282805 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 52000-440-02 | 2.5% Menthol PAIN RELIEF | 57 g in 1 TUBE | GEL | 57 | | 1 |
| 52000-440-02 | 2.5% Menthol PAIN RELIEF | 1 in 1 BOX | GEL | 1 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 52000-440-02 | 52000044002 | 1 TUBE in 1 BOX (52000-440-02) / 57 g in 1 TUBE | 1 tube | 2026-01-19 | No | No | Current |