Walgreens Maximum Strength Jock Itch Antifungal
- Product NDC
- 23667-807
- 11-digit product format
- 236670807
- Labeler code
- 23667
- Product ID
- 23667-807_0b826cf7-a501-806c-e063-6294a90a2f5f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TOLNAFTATE
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Formulated Solutions, LLC
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2017-01-20
- 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
- Walgreens Maximum Strength Jock Itch 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 | 705934 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 23667-807-01 | Walgreens Maximum Strength Jock Itch Antifungal | 130 g in 1 CAN | SPRAY | 130 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 23667-807 | WALGREENS MAXIMUM STRENGTH JOCK ITCH ANTIFUNGAL (TOLNAFTATE) SPRAY [FORMULATED SOLUTIONS, LLC] | 2 | Current NDC, Legacy NDC, 1 package rows | 20231207_46c5fa20-12a8-272e-e054-00144ff8d46c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 23667-807-01 | 23667080701 | 130 g in 1 CAN (23667-807-01) | 130 g | 2017-01-20 | 0000-00-00 | No | No | Current |