Lidocaine
- Product NDC
- 73581-900
- 11-digit product format
- 735810900
- Labeler code
- 73581
- Product ID
- 73581-900_5b9c949b-bde0-7db8-e063-6294a90ae5c1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lidocaine
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- YYBA CORP
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-09-16
- Substance
- LIDOCAINE
- Active strength
- 80 mg/mL
- 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
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Lidocaine
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| LIDOCAINE | 80 mg/mL |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 73581-900-01 | 73581090001 | 1 BOTTLE in 1 CARTON (73581-900-01) / 30 mL in 1 BOTTLE | 1 bottle | 2026-09-16 | No | No | Current |