Dermoplast Pain Relieving is a Topical Spray in the Human Otc Drug category. It is labeled and distributed by Advantice Health, Llc. The primary component is Benzocaine; Levomenthol.
| Product ID | 16864-680_091fe5c1-550f-47dc-83d6-3d792fd22dcb |
| NDC | 16864-680 |
| Product Type | Human Otc Drug |
| Proprietary Name | Dermoplast Pain Relieving |
| Generic Name | Benzocaine And Levomenthol |
| Dosage Form | Spray |
| Route of Administration | TOPICAL |
| Marketing Start Date | 2014-01-01 |
| Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
| Application Number | part348 |
| Labeler Name | Advantice Health, LLC |
| Substance Name | BENZOCAINE; LEVOMENTHOL |
| Active Ingredient Strength | 200 mg/g; mg/g |
| NDC Exclude Flag | N |
| Listing Certified Through | 2022-12-31 |
| Marketing Start Date | 2014-01-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC MONOGRAPH NOT FINAL |
| Application Number | part348 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | GM |
| Marketing Start Date | 2014-01-01 |
| Marketing Category | OTC MONOGRAPH NOT FINAL |
| Application Number | part348 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | GM |
| Marketing Start Date | 2014-01-01 |
| Ingredient | Strength |
|---|---|
| BENZOCAINE | 200 mg/g |
| SPL SET ID: | 2347f0b8-d463-422d-8583-65624d9a1a91 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 16864-680 | Dermoplast Pain Relieving | BENZOCAINE and LEVOMENTHOL |
| 16864-690 | Dermoplast Pain relieving | BENZOCAINE, MENTHOL |
| 16864-682 | Dermoplast Insect Itch and Sting Relief | BENZOCAINE and LEVOMENTHOL |
| 16864-681 | Dermoplast Sunburn and Burn Relief | benzocaine and levomenthol |