CLARUS AC Antifungal Solution
- Product NDC
- 44577-128
- 11-digit product format
- 445770128
- Labeler code
- 44577
- Product ID
- 44577-128_09d7052e-ec64-ef60-e063-6294a90af214
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TOLNAFTATE
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Clinical Therapeutic Solutions
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-03-01
- Substance
- TOLNAFTATE
- Active strength
- 10 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- CLARUS AC Antifungal Solution
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TOLNAFTATE | 10 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 06KB629TKV |
| Rxcui | 313423 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 44577-128-00 | CLARUS AC Antifungal Solution | 15 g in 1 TUBE | LIQUID | 15 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 44577-128 | CLARUS AC ANTIFUNGAL SOLUTION (TOLNAFTATE) LIQUID [CLINICAL THERAPEUTIC SOLUTIONS] | 2 | Current NDC, Legacy NDC, 1 package rows | 20231111_28ab9f1b-65cd-4405-a9a3-f3c9b836693d.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 |
|---|
| 44577-128-00 | 44577012800 | 15 g in 1 TUBE (44577-128-00) | 15 g | 2021-03-01 | 0000-00-00 | No | No | Current |