Dermoplast Sunburn and Burn Relief
- Product NDC
- 16864-681
- 11-digit product format
- 168640681
- Labeler code
- 16864
- Product ID
- 16864-681_b30118b0-b328-4782-8f68-8f99ab19fcd7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- benzocaine and levomenthol
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Advantice Health, LLC
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2021-05-15
- Marketing end
- 0000-00-00
- Substance
- BENZOCAINE; LEVOMENTHOL
- Active strength
- 200 mg/g; mg/g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 16864-681-01 | Dermoplast Sunburn and Burn Relief | 78 g in 1 CAN | SPRAY | 78 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 16864-681 | DERMOPLAST SUNBURN AND BURN RELIEF (BENZOCAINE AND LEVOMENTHOL) SPRAY [ADVANTICE HEALTH, LLC] | 3 | Legacy NDC, 1 package rows | 20241215_5d9f8ac1-cf42-4e30-bb3f-f59723f95b1a.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 |
|---|
| 16864-681-01 | 16864068101 | 78 g in 1 CAN (16864-681-01) | 78 g | 2021-05-15 | 0000-00-00 | No | No | Current |