ProClearz Laser Antifungal
- Product NDC
- 29784-183
- 11-digit product format
- 297840183
- Labeler code
- 29784
- Product ID
- 29784-183_4988109f-6e4b-0acb-e063-6294a90a419e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TOLNAFTATE
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Rooftop Consumer Health, inc
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-01-01
- Substance
- TOLNAFTATE
- Active strength
- 10 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ProClearz Laser Antifungal
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TOLNAFTATE | 10 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 06KB629TKV |
| Rxcui | 313421, 2700695 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 29784-183-01 | ProClearz Laser Antifungal | 85 g in 1 BOTTLE, SPRAY | LIQUID | 85 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 29784-183 | PROCLEARZ LASER ANTIFUNGAL (TOLNAFTATE) LIQUID [ROOFTOP CONSUMER HEALTH, INC] | 2 | Current NDC, 1 package rows | 20250105_53648135-7b79-4775-993b-48fa1298b747.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 |
|---|
| 29784-183-01 | 29784018301 | 85 g in 1 BOTTLE, SPRAY (29784-183-01) | 85 g | 2025-01-01 | No | No | Current |