APUREE Nailtific Extra-Max Strength Nighttime Antifungal
- Product NDC
- 84167-479
- 11-digit product format
- 841670479
- Labeler code
- 84167
- Product ID
- 84167-479_4e3e8895-34b5-de69-e063-6294a90a5532
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- APUREE Nailtific Extra-Max Strength Nighttime Antifungal
- 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
- Active strength
- 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 Nighttime Antifungal
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TOLNAFTATE | 1 g/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 06KB629TKV |
| Rxcui | 313423 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84167-479-02 | APUREE Nailtific Extra-Max Strength Nighttime Antifungal | 1 in 1 BOX | LIQUID | 1 | | 1 |
| 84167-479-02 | APUREE Nailtific Extra-Max Strength Nighttime Antifungal | 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 |
|---|
| 84167-479-02 | 84167047902 | 1 VIAL, SINGLE-USE in 1 BOX (84167-479-02) / 30 LIQUID in 1 VIAL, SINGLE-USE | 2026-03-30 | No | No | Current |