Tinactin
- Product NDC
- 11523-0138
- 11-digit product format
- 115230138
- Labeler code
- 11523
- Product ID
- 11523-0138_4526e2eb-ee8a-3ac4-e063-6394a90a133f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Tolnaftate
- Dosage form
- AEROSOL, POWDER
- Route
- TOPICAL
- Labeler
- Bayer HealthCare LLC
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-03-01
- 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
- Tinactin
- Brand name suffix
- Jock Itch
- 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, 705936 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 11523-0138-1 | TinactinJock Itch | 133 g in 1 CAN | AEROSOL, POWDER | 133 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11523-0138 | TINACTIN JOCK ITCH (TOLNAFTATE) AEROSOL, POWDER [BAYER HEALTHCARE LLC] | 1 | Current NDC, 1 package rows | 20240531_163ab4df-6e4a-6239-e063-6294a90a1cd0.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 |
|---|
| 11523-0138-1 | 11523013801 | 133 g in 1 CAN (11523-0138-1) | 133 g | 2024-03-01 | No | No | Current |