PAIN-X
- Product NDC
- 80489-003
- 11-digit product format
- 804890003
- Labeler code
- 80489
- Product ID
- 80489-003_2b51e8c1-1805-573d-e063-6294a90a2f58
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- OL PHARMA TECH,LLC
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-01-01
- Substance
- MENTHOL, UNSPECIFIED FORM
- Active strength
- 25 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- PAIN-X
- Listing expiration
- 2026-12-31
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#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 80489-003 | PAIN-X (MENTHOL) GEL [OL PHARMA TECH,LLC] | 4 | Current NDC, Legacy NDC, 4 package rows | 20250112_b22bb19a-14e5-3d32-e053-2a95a90ae520.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 80489-003-01 | 80489000301 | 1 TUBE in 1 CARTON (80489-003-01) / 28.3 g in 1 TUBE | 1 tube | 2021-01-01 | 0000-00-00 | No | No | Current |
| 80489-003-02 | 80489000302 | 1 TUBE in 1 CARTON (80489-003-02) / 49.6 g in 1 TUBE | 1 tube | 2021-01-01 | 0000-00-00 | No | No | Current |