NuLido
- Product NDC
- 53149-2100
- 11-digit product format
- 531492100
- Labeler code
- 53149
- Product ID
- 53149-2100_5b0d2255-bb8b-4b79-8c92-249bd776115c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lidocaine Hydrocloride 4%
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- All Pharma LLC
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-10-01
- Marketing end
- 0000-00-00
- Substance
- LIDOCAINE; MENTHOL
- Active strength
- 4 mg/mL; mg/mL
- 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 |
|---|
| 53149-2100-4 | NuLido | 120 mL in 1 TUBE | GEL | 120 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53149-2100 | NULIDO (LIDOCAINE HYDROCLORIDE 4%) GEL [ALL PHARMA LLC] | 3 | Legacy NDC, 1 package rows | 20220121_57904d54-494d-4859-8a8f-619e662d7fef.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 53149-2100-4 | 53149210004 | 120 mL in 1 TUBE (53149-2100-4) | 120 ml | 2017-10-01 | 0000-00-00 | No | No | Current |