MyDerm Bite Relief
- Product NDC
- 72667-019
- 11-digit product format
- 726670019
- Labeler code
- 72667
- Product ID
- 72667-019_2d07a8c9-17a4-1727-e063-6394a90a801d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzocaine
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Inspec Solutions LLC.
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-12-14
- Substance
- BENZOCAINE
- Active strength
- 5 g/100g
- 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
- MyDerm Bite Relief
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZOCAINE | 5 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | U3RSY48JW5 |
| Rxcui | 251295 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72667-019-01 | MyDerm Bite Relief | 50 g in 1 TUBE | OINTMENT | 50 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72667-019 | MYDERM BITE RELIEF (BENZOCAINE) OINTMENT [INSPEC SOLUTIONS LLC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20250202_88615668-16b5-7840-e053-2a95a90a9208.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 |
|---|
| 72667-019-01 | 72667001901 | 50 g in 1 TUBE (72667-019-01) | 50 g | 2021-12-14 | 0000-00-00 | No | No | Current |