Up and Up Antifungal
- Product NDC
- 82442-020
- 11-digit product format
- 824420020
- Labeler code
- 82442
- Product ID
- 82442-020_5983ff26-abde-4b25-96ba-3303397aad8f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Tolnaftate 1%
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Target Corporation
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-08-01
- Substance
- TOLNAFTATE
- Active strength
- 10 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Up and Up Antifungal
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TOLNAFTATE | 10 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 06KB629TKV |
| Rxcui | 103951 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82442-020-28 | Up and Up Antifungal | 1 in 1 CARTON | CREAM | 1 | | 2 |
| 82442-020-28 | Up and Up Antifungal | 28 g in 1 TUBE | CREAM | 28 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 82442-020 | UP AND UP ANTIFUNGAL (TOLNAFTATE 1%) CREAM [TARGET CORPORATION] | 2 | Current NDC, 2 package rows | 20240802_8f54c8c7-6771-49c3-b429-53aa6df54dc5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82442-020-28 | 82442002028 | 1 TUBE in 1 CARTON (82442-020-28) / 28 g in 1 TUBE | 1 tube | 2024-08-01 | No | No | Historical |