Lightning Pain Relief
- Product NDC
- 63742-013
- 11-digit product format
- 637420013
- Labeler code
- 63742
- Product ID
- 63742-013_4c143af2-cd3f-2fc8-e063-6394a90a40b7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Clinical Resolution Laboratory, Inc.
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-05-01
- Substance
- MENTHOL
- Active strength
- 40 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
- Lightning Pain Relief
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | 40 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
| Rxcui | 1148430 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63742-013-00 | Lightning Pain Relief | 65 g in 1 BOTTLE | CREAM | 65 | | 5 |
| 63742-013-01 | Lightning Pain Relief | 101 g in 1 BOTTLE | CREAM | 101 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63742-013 | LIGHTNING PAIN RELIEF (MENTHOL) CREAM [CLINICAL RESOLUTION LABORATORY, INC.] | 4 | Current NDC, Legacy NDC, 2 package rows | 20240103_80af21f5-dba8-42b0-8a65-ac5a94d83ca8.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 |
|---|
| 63742-013-00 | 63742001300 | 65 g in 1 BOTTLE (63742-013-00) | 65 g | 2019-05-01 | 0000-00-00 | No | No | Current |
| 63742-013-01 | 63742001301 | 101 g in 1 BOTTLE (63742-013-01) | 101 g | 2019-05-01 | 0000-00-00 | No | No | Current |