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
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 | Historical |