femmesil Ultra Therapy
- Product NDC
- 24909-050
- 11-digit product format
- 249090050
- Labeler code
- 24909
- Product ID
- 24909-050_3d36794a-07d1-860c-e063-6294a90a6e8f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Clotrimazole
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Aidance Scientific, Inc.
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-08-25
- Substance
- CLOTRIMAZOLE
- Active strength
- 1 g/100g
- 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
- femmesil Ultra Therapy
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CLOTRIMAZOLE | 1 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | G07GZ97H65 |
| Rxcui | 2722226 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 24909-050-28 | femmesil Ultra Therapy | 28 g in 1 TUBE | OINTMENT | 28 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 24909-050-28 | 24909005028 | 28 g in 1 TUBE (24909-050-28) | 28 g | 2025-08-25 | No | No | Current |