Hampton Sun 0.5% Lidocaine Gel
- Product NDC
- 72667-053
- 11-digit product format
- 726670053
- Labeler code
- 72667
- Product ID
- 72667-053_e2642625-0074-0784-e053-2995a90a4a51
- 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
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 72667-053-01 | 72667005301 | 177 mL in 1 TUBE (72667-053-01) | 177 ml | 2022-06-25 | 0000-00-00 | No | No | Current |