Point Relief cold Spot Pain Relieving roll-on
- Product NDC
- 51452-037
- 11-digit product format
- 514520037
- Labeler code
- 51452
- Product ID
- 51452-037_0973b73d-5dde-0986-e063-6294a90a5917
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Fabrication Enterprises
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-04-01
- Substance
- MENTHOL
- Active strength
- 140 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
- Point Relief cold Spot Pain Relieving roll-on
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | 140 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
| Rxcui | 2121681, 2121685 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51452-037-06 | Point Relief cold Spot Pain Relieving roll-on | 90 mL in 1 CONTAINER | LIQUID | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51452-037 | POINT RELIEF COLD SPOT PAIN RELIEVING ROLL-ON (MENTHOL) LIQUID [FABRICATION ENTERPRISES] | 2 | Current NDC, Legacy NDC, 1 package rows | 20231106_3f1db0ad-aaa8-4e14-9349-45057e0fb4a6.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 |
|---|
| 51452-037-06 | 51452003706 | 90 mL in 1 CONTAINER (51452-037-06) | 90 ml | 2019-04-01 | 0000-00-00 | No | No | Current |