Tolnaftate
- Product NDC
- 0363-0186
- 11-digit product format
- 003630186
- Labeler code
- 0363
- Product ID
- 0363-0186_be4e0d04-6a8a-df68-e053-2a95a90a7a82
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Anti-Fungal Liquid Maximum Strength
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Walgreen Company
- Application
- part333C
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-03-24
- Marketing end
- 0000-00-00
- Substance
- TOLNAFTATE
- Active strength
- 0 g/30mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0363-0186 | TOLNAFTATE (ANTI-FUNGAL LIQUID MAXIMUM STRENGTH) LIQUID [WALGREEN COMPANY] | 5 | Legacy NDC | 20241206_be4df7d1-4d96-9426-e053-2a95a90a7d2b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0363-0186-30 | 00363018630 | 30 mL in 1 BOTTLE, WITH APPLICATOR (0363-0186-30) | 30 ml | 2021-03-24 | 0000-00-00 | No | No | Current |