NDC 29784-181-01 - ProClearz Maximum Strength Fungal Shield Brush-on Antifungal
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 29784-181
- Requested NDC
- 29784-181-01
- Package NDCs from labels
- 29784-181-01, 29784-181-02
- Manufacturer
- Rooftop Consumer Health, Inc.
- Effective date
- 2026-03-02
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| ProClearz Maximum Strength Fungal Sheild Anti-Fungal Brush-On Solution | Rooftop Consumer Health, Inc. | 2026-03-02 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 29784-181-01 | ProClearzMaximum Strength Fungal Shield Brush-on Antifungal | 30 mL in 1 BOTTLE, WITH APPLICATOR | SOLUTION | 30 | 38 | |
| 29784-181-02 | ProClearzMaximum Strength Fungal Shield Brush-on Antifungal | 1 in 1 BOX | SOLUTION | 1 | 38 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 29784-181 | PROCLEARZ MAXIMUM STRENGTH FUNGAL SHIELD BRUSH-ON ANTIFUNGAL (TOLNAFTATE) SOLUTION [ROOFTOP CONSUMER HEALTH, INC.] | 36 | Current NDC, Legacy NDC, 2 package rows | 20250105_4d451e87-c25b-49cf-92b8-747b053930c2.zip |
DailyMed Socrata Ingredients#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Micatin | MICONAZOLE NITRATE | WellSpring Pharmaceutical Corporation | 96c56ba1-c3a8-48ce-ab58-550959485e3c | 2016-04-07 | Warnings | M005 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.