Dermoplast Pain relieving
- Product NDC
- 16864-690
- 11-digit product format
- 168640690
- Labeler code
- 16864
- Product ID
- 16864-690_0d12185e-8d41-7d76-e063-6294a90a2cf4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BENZOCAINE, MENTHOL
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Advantice Health
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-03-18
- Substance
- BENZOCAINE; MENTHOL
- Active strength
- 200; 5 mg/g; mg/g
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Dermoplast Pain relieving
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZOCAINE | 200 mg/g |
| MENTHOL | 5 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | U3RSY48JW5, L7T10EIP3A |
| Rxcui | 199864, 763484 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 16864-690-01 | Dermoplast Pain relieving | 78 g in 1 CAN | SPRAY | 78 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 16864-690 | DERMOPLAST PAIN RELIEVING (BENZOCAINE, MENTHOL) SPRAY [ADVANTICE HEALTH] | 2 | Current NDC, Legacy NDC, 1 package rows | 20231222_dad00c95-4e11-3eec-e053-2a95a90a7a18.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 |
|---|
| 16864-690-01 | 16864069001 | 78 g in 1 CAN (16864-690-01) | 78 g | 2022-03-18 | 0000-00-00 | No | No | Current |