Point relief Lidospot
- Product NDC
- 51452-173
- 11-digit product format
- 514520173
- Labeler code
- 51452
- Product ID
- 51452-173_db72a44e-a828-9fa5-e053-2995a90aa7de
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lidocaine, Menthol
- Dosage form
- PATCH
- Route
- TOPICAL
- Labeler
- Fabrication Enterprises
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2022-04-05
- Marketing end
- 0000-00-00
- Substance
- LIDOCAINE; MENTHOL
- Active strength
- 0 g/3g; g/3g
- Pharmacologic classes
- Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51452-173-01 | Point relief Lidospot | 3 g in 1 PATCH | PATCH | 3 | | 1 |
| 51452-173-05 | Point relief Lidospot | 5 in 1 POUCH | PATCH | 5 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51452-173 | POINT RELIEF LIDOSPOT (LIDOCAINE, MENTHOL) PATCH [FABRICATION ENTERPRISES] | 1 | Legacy NDC, 2 package rows | 20220405_db72a44e-a827-9fa5-e053-2995a90aa7de.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 |
|---|
| 51452-173-01 | 51452017301 | 3 g in 1 PATCH | 3 g | | | | | Historical |
| 51452-173-05 | 51452017305 | 5 PATCH in 1 POUCH (51452-173-05) > 3 g in 1 PATCH (51452-173-01) | 5 patch | 2022-04-05 | 0000-00-00 | No | No | Current |