Nailene Antifungal Treatment
- Product NDC
- 60193-102
- 11-digit product format
- 601930102
- Labeler code
- 60193
- Product ID
- 60193-102_e078e140-0b97-46e9-99c8-de9c5593a5bb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TOLNAFTATE
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Pacific World Corporation
- Application
- part333C
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2013-04-24
- Marketing end
- 0000-00-00
- Substance
- TOLNAFTATE
- Active strength
- 10 mg/mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 60193-102-02 | Nailene Antifungal Treatment | 18 mL in 1 BOTTLE, WITH APPLICATOR | LIQUID | 18 | | 3 |
| 60193-102-02 | Nailene Antifungal Treatment | 1 in 1 CARTON | LIQUID | 1 | | 3 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60193-102 | NAILENE ANTIFUNGAL TREATMENT (TOLNAFTATE) LIQUID [PACIFIC WORLD CORPORATION] | 3 | Legacy NDC, 2 package rows | 20141021_ae22a4f1-77bd-4b37-bf3c-24f402e15bf0.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 60193-102-02 | 60193010202 | 18 mL in 1 BOTTLE, WITH APPLICATOR | 18 ml | Historical |