Sunburn Relief
- Product NDC
- 55910-177
- 11-digit product format
- 559100177
- Labeler code
- 55910
- Product ID
- 55910-177_4c0e990c-be02-8260-e063-6294a90a2dbb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lidocaine HCl 0.5%
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Old East Main Co.
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-12-30
- 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
- Sunburn Relief
- 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 |
|---|
| 55910-177-34 | Sunburn Relief | 226 g in 1 BOTTLE, PLASTIC | GEL | 226 | | 11 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55910-177 | SUNBURN RELIEF (LIDOCAINE HCL 0.5%) GEL [OLD EAST MAIN CO] | 10 | Current NDC, Legacy NDC, 1 package rows | 20250302_49173ec8-c94a-44c9-8a13-0f4b01b96cd6.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55910-177-34 | 55910017734 | 226 g in 1 BOTTLE, PLASTIC (55910-177-34) | 226 g | 2019-12-30 | 0000-00-00 | No | No | Current |