FlexDermal Pain Relieving Roll-On
- Product NDC
- 84197-867
- 11-digit product format
- 841970867
- Labeler code
- 84197
- Product ID
- 84197-867_2d76e34f-c583-4eae-e063-6294a90a5de5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- SOLVADERM LLC
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-01-24
- Substance
- MENTHOL
- Active strength
- 20 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- FlexDermal Pain Relieving Roll-On
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | 20 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84197-867-00 | FlexDermal Pain Relieving Roll-On | 90 mL in 1 BOTTLE | LIQUID | 90 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 84197-867 | FLEXDERMAL PAIN RELIEVING ROLL-ON (MENTHOL) LIQUID [SOLVADERM LLC] | 1 | Current NDC, 1 package rows | 20250209_d4d8050e-0761-4491-8635-39c806701eb5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84197-867-00 | 84197086700 | 90 mL in 1 BOTTLE (84197-867-00) | 90 ml | 2025-01-24 | No | No | Historical |