Fungal Nail Treatment
- Product NDC
- 84778-075
- 11-digit product format
- 847780075
- Labeler code
- 84778
- Product ID
- 84778-075_38d9d0c2-f102-a001-e063-6394a90a9dd5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fungal Nail Treatment
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Guangzhou Yixin Cross-border E-commerce Co., Ltd.
- Application
- M029
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-06-14
- Substance
- EUCALYPTUS GLOBULUS WHOLE
- Active strength
- 1 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Fungal Nail Treatment
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| EUCALYPTUS GLOBULUS WHOLE | 1 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | SI1P2XF3M3 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84778-075-01 | Fungal Nail Treatment | 15 g in 1 BOTTLE | LIQUID | 15 | | 3 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84778-075-01 | 84778007501 | 15 g in 1 BOTTLE (84778-075-01) | 15 g | 2025-06-14 | No | No | Current |