APUREE Nailtific Extra-Max Strength Daytime Antigungal
- Product NDC
- 84167-423
- 11-digit product format
- 841670423
- Labeler code
- 84167
- Product ID
- 84167-423_4e3d226b-57f2-75a6-e063-6394a90a96cd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- APUREE Nailtific Extra-Max Strength Daytime Antigungal
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Guangzhou Meixi Biotechnology Co., Ltd.
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-03-30
- Substance
- TOLNAFTATE; UNDECYLENIC ACID
- Active strength
- 1; 25 g/1; g/1
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- APUREE Nailtific Extra-Max Strength Daytime Antigungal
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TOLNAFTATE | 1 g/1 |
| UNDECYLENIC ACID | 25 g/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 06KB629TKV, K3D86KJ24N |
| Rxcui | 2691548 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84167-423-01 | APUREE Nailtific Extra-Max Strength Daytime Antigungal | 1 in 1 BOX | LIQUID | 1 | | 1 |
| 84167-423-01 | APUREE Nailtific Extra-Max Strength Daytime Antigungal | 30 in 1 VIAL, SINGLE-USE | LIQUID | 30 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 84167-423-01 | 84167042301 | 1 VIAL, SINGLE-USE in 1 BOX (84167-423-01) / 30 LIQUID in 1 VIAL, SINGLE-USE | 2026-03-30 | No | No | Current |