Mango Bay 0.5% Lidocaine Gel
- Product NDC
- 72667-042
- 11-digit product format
- 726670042
- Labeler code
- 72667
- Product ID
- 72667-042_e260fcb6-7303-75cf-e053-2a95a90a72f1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lidocaine
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Inspec Solutions LLC.
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2022-06-25
- Marketing end
- 0000-00-00
- Substance
- LIDOCAINE HYDROCHLORIDE
- Active strength
- 1 g/100mL
- 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
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 72667-042 | D | Discontinued by firm | 2026-10-05 | ||
| excluded package | package | 72667-042 | 72667-042-01 | D | Discontinued by firm | 2026-10-05 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 72667-042-01 | 72667004201 | 237 mL in 1 BOTTLE, PLASTIC (72667-042-01) | 237 ml | 2022-06-25 | 0000-00-00 | No | No | Current |