Lidoxi
- Product NDC
- 87239-1111
- 11-digit product format
- 872391111
- Labeler code
- 87239
- Product ID
- 87239-1111_513c517e-c099-02aa-e063-6294a90ac8a4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lidocaine
- Dosage form
- OINTMENT
- Route
- CUTANEOUS
- Labeler
- T&T Pharma Holdings LLC
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-05-07
- Substance
- LIDOCAINE
- Active strength
- .04 g/g
- Pharmacologic classes
- Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Lidoxi
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LIDOCAINE | .04 g/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 98PI200987 |
| Rxcui | 2559400 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 87239-1111-1 | Lidoxi | 92 g in 1 TUBE, WITH APPLICATOR | OINTMENT | 92 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 87239-1111-1 | 87239111101 | 92 g in 1 TUBE, WITH APPLICATOR (87239-1111-1) | 92 g | 2026-05-07 | No | No | Current |