Nailtific Daytime Treatment Antifungal Pen Refill
- Product NDC
- 84167-012
- 11-digit product format
- 841670012
- Labeler code
- 84167
- Product ID
- 84167-012_4f29bfc9-9cf1-7289-e063-6394a90a37a2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Nailtific Daytime Treatment Antifungal Pen Refill
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Guangzhou Meixi Biotechnology Co., Ltd.
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-10-30
- Substance
- TOLNAFTATE; UNDECYLENIC ACID
- Active strength
- .06; 1.5 g/6mL; g/6mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Nailtific Daytime Treatment Antifungal Pen Refill
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TOLNAFTATE | .06 g/6mL |
| UNDECYLENIC ACID | 1.5 g/6mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 06KB629TKV, K3D86KJ24N |
| Rxcui | 2691548 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84167-012-27 | Nailtific Daytime Treatment Antifungal Pen Refill | 50 mL in 1 BOTTLE | LIQUID | 50 | | 3 |
| 84167-012-27 | Nailtific Daytime Treatment Antifungal Pen Refill | 1 in 1 BOTTLE | LIQUID | 1 | | 3 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84167-012-27 | 84167001227 | 1 BOTTLE in 1 BOTTLE (84167-012-27) / 50 mL in 1 BOTTLE | 1 bottle | 2025-10-30 | No | No | Current |