APUREE Nailtific Extra-Max Strength Antigungal
- Product NDC
- 84167-662
- 11-digit product format
- 841670662
- Labeler code
- 84167
- Product ID
- 84167-662_4a633da8-dcbb-349c-e063-6294a90a7702
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- APUREE Nailtific Extra-Max Strength Antigungal
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Guangzhou Meixi Biotechnology Co., Ltd.
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-02-09
- Substance
- TOLNAFTATE; UNDECYLENIC ACID
- Active strength
- .01; .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 Antigungal
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TOLNAFTATE | .01 g/1 |
| UNDECYLENIC ACID | .25 g/1 |
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 |
|---|
| 84167-662-23 | APUREE Nailtific Extra-Max Strength Antigungal | 1 in 1 BOTTLE, PLASTIC | LIQUID | 1 | | 1 |
| 84167-662-23 | APUREE Nailtific Extra-Max Strength Antigungal | 5 in 1 BOX | LIQUID | 5 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 84167-662-23 | 84167066223 | 5 BOTTLE, PLASTIC in 1 BOX (84167-662-23) / 1 LIQUID in 1 BOTTLE, PLASTIC | 2026-02-09 | No | No | Current |