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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Pain Relieving Gel
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LIDOCAINE HYDROCHLORIDE | 5 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | V13007Z41A |
| Rxcui | 1011849 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 83324-183-08 | Pain Relieving Gel | 226 g in 1 BOTTLE, PLASTIC | GEL | 226 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 83324-183 | PAIN RELIEVING GEL (LIDOCAINE HYDROCHLORIDE) GEL [CHAIN DRUG MARKETING ASSOCIATION] | 2 | Current NDC, 1 package rows | 20250313_b55b7253-2fd2-45cc-b94c-e92395ab0d2b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| 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 | Current |