Forticept Antifungal Foot Gel
- Product NDC
- 72127-0806
- 11-digit product format
- 721270806
- Labeler code
- 72127
- Product ID
- 72127-0806_ed6062d8-e888-413c-bd50-6c6ed86d8a19
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Clotrimazole
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Lidan, Inc.
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-04-12
- Substance
- CLOTRIMAZOLE
- Active strength
- .01 kg/kg
- Pharmacologic classes
- Azole Antifungal [EPC], Azoles [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Forticept Antifungal Foot Gel
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CLOTRIMAZOLE | .01 kg/kg |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | G07GZ97H65 |
| Rxcui | 1049535 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72127-0806-0 | Forticept Antifungal Foot Gel | 0.085 kg in 1 TUBE | GEL | 0.085 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72127-0806 | FORTICEPT ANTIFUNGAL FOOT GEL (CLOTRIMAZOLE) GEL [LIDAN, INC.] | 2 | Current NDC, 1 package rows | 20250327_1b5851fc-ae73-4e54-bb62-3ff928628b97.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72127-0806-0 | 72127080600 | .085 kg in 1 TUBE (72127-0806-0) | 2020-04-12 | No | No | Current |