Pain Relieving Gel
- Product NDC
- 83324-183
- 11-digit product format
- 833240183
- Labeler code
- 83324
- Product ID
- 83324-183_4bcf38d5-ccde-3ab0-e063-6294a90a3eb4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- LIDOCAINE HYDROCHLORIDE
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Chain Drug Marketing Association
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-07-08
- Substance
- LIDOCAINE HYDROCHLORIDE
- Active strength
- 5 mg/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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| V13007Z41A | LIDOCAINE HYDROCHLORIDE | 6108-05-0 | LIDOCAINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 83324-183-08 | 83324018308 | 226 g in 1 BOTTLE, PLASTIC (83324-183-08) | 226 g | 2024-07-08 | No | No | Historical |