Point Relief Cold Spot Pain Relieving
- Product NDC
- 51452-036
- 11-digit product format
- 514520036
- Labeler code
- 51452
- Product ID
- 51452-036_0973ce0d-48e1-5977-e063-6394a90ad88e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Fabrication Enterprises
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-04-01
- Substance
- MENTHOL
- Active strength
- 120 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
- Point Relief Cold Spot Pain Relieving
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | 120 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
| Rxcui | 2121666, 2121669 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51452-036-06 | Point Relief Cold Spot Pain Relieving | 5 g in 1 PACKET | GEL | 5 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51452-036 | POINT RELIEF COLD SPOT PAIN RELIEVING (MENTHOL) GEL [FABRICATION ENTERPRISES] | 2 | Current NDC, Legacy NDC, 1 package rows | 20231106_391af69f-74aa-48cf-bc96-75e5c4e0e445.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 |
|---|
| 51452-036-06 | 51452003606 | 5 g in 1 PACKET (51452-036-06) | 5 g | 2019-04-01 | 0000-00-00 | No | No | Current |