Dr. Zenovia Spot Treatment
- Product NDC
- 51326-802
- 11-digit product format
- 513260802
- Labeler code
- 51326
- Product ID
- 51326-802_470d894e-af84-4370-880c-16725870d808
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzoyl Peroxide
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Topiderm, Inc.
- Application
- M006
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-06-11
- Substance
- BENZOYL PEROXIDE
- Active strength
- 50 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Dr. Zenovia Spot Treatment
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZOYL PEROXIDE | 50 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | W9WZN9A0GM |
| Rxcui | 1488689 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51326-802-01 | Dr. Zenovia Spot Treatment | 1 in 1 BOX | LIQUID | 1 | | 2 |
| 51326-802-01 | Dr. Zenovia Spot Treatment | 15 mL in 1 BOTTLE | LIQUID | 15 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51326-802 | DR. ZENOVIA SPOT TREATMENT (BENZOYL PEROXIDE) LIQUID [TOPIDERM, INC.] | 2 | Current NDC, 2 package rows | 20240628_dfdb3d8e-4d39-4ce4-851f-80b11972ca9e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 51326-802-01 | 51326080201 | 1 BOTTLE in 1 BOX (51326-802-01) / 15 mL in 1 BOTTLE | 1 bottle | 2024-06-11 | No | No | Current |