SERYNTH Clotrimazole
- Product NDC
- 85248-101
- 11-digit product format
- 852480101
- Labeler code
- 85248
- Product ID
- 85248-101_5729a4d3-1503-946f-e063-6294a90a6384
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Clotrimazole1% Clotrimazole
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Jiangxi Yudexi Pharmaceutical Co., LTD
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-02-08
- Substance
- CLOTRIMAZOLE
- Active strength
- 1 g/100g
- Pharmacologic classes
- Azole Antifungal [EPC], Azoles [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- SERYNTH Clotrimazole
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| CLOTRIMAZOLE | 1 g/100g |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| G07GZ97H65 | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 309367 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 4a4b304a-1acc-9185-e063-6394a90a1176 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| b64d2752-34ef-378a-1f4f-8bff32b0d1ae | Product name | 4 | 20250626 |
| cb7783e0-feaa-7e56-fb3b-d43b6efa77c9 | Product name | 2 | 20250121 |
| f31c883b-7ebf-1c60-f3b6-4ba41e8ff7a6 | Product name | 2 | 20151106 |
| f5395dd2-4395-d8c6-3477-8c2d4a2f951c | Product name | 1 | 20140508 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 85248-101-01 | SERYNTH Clotrimazole | 30 g in 1 BOTTLE | CREAM | 30 | 1 | |
| 85248-101-02 | SERYNTH Clotrimazole | 60 g in 1 BOTTLE | CREAM | 60 | 1 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Clotrimazole | CLOTRIMAZOLE | AvPAK | 3ca3b475-7b69-442a-e063-6294a90a7b3f | 2025-08-18 | Warnings | M005 |
| Formula 3 | TOLNAFTATE | The Tetra Corporation | 0895274b-a09d-4264-a43f-852e44eb3163 | 2025-08-18 | Warnings | M005 |
| Formula 7 - The Solution | TOLNAFTATE | The Tetra Corporation | 18619649-7f79-4b6e-8b7c-69d70365d557 | 2025-08-18 | Warnings | M005 |
| GlyCylic | SALICYLIC ACID | The Tetra Corporation | 501d3ba9-ba42-4c1c-983b-492adaee039d | 2025-08-18 | Warnings | M005 |
| SupreH Ringworm Treatment Balm | SUPREH RINGWORM TREATMENT BALM | Shenzhen Xinxin Yunhai Technology Co., Ltd. | 3c77222b-d92e-84b0-e063-6294a90aadd7 | 2025-08-16 | Warnings | M005 |
| OetMoe Antifungal Solution | OETMOE ANTIFUNGAL SOLUTION | Shenzhen Earth Surface Trading Co., Ltd. | 3c26d917-4186-6f02-e063-6394a90a99f6 | 2025-08-12 | Warnings | M005 |
| Cureforte Anti Fungal Foot Care | ANTI FUNGAL FOOT CARE DROPS | STEEL CITY HEALTH PRIVATE LIMITED | 39f762a6-9d0c-8ded-e063-6394a90a3659 | 2025-08-11 | Warnings | M005 |
| Derman Antifungal Powder Tolnaftate | TOLNAFTATE | Taisho Pharmaceutical California Inc. | 3a854765-740c-4719-8abf-4b3f932cdee0 | 2025-08-07 | Warnings | M005 |
| Derman antifungal cream | TOLNAFTATE | Taisho Pharmaceutical California Inc. | 15d9b3c9-01af-4083-a1bc-014505d8798d | 2025-08-07 | Warnings | M005 |
| Maximum Strength Antifungal Liquid | TOLNAFTATE | Hudson Health LLC | 24b22794-f9f8-6f32-e063-6394a90aec98 | 2025-08-07 | Warnings | M005 |
| Toe Area Treatment | TOLNAFTATE | CVS | 17681cc8-fbb1-a0cf-e063-6294a90add18 | 2025-08-07 | Warnings | M005 |
| Antifungal Liquid | TOLNAFTATE | Family Dollar Services, Inc | 178e7b3f-949f-3f51-e063-6294a90a9395 | 2025-08-07 | Warnings | M005 |
| Antifungal Liquid | TOLNAFTATE | LEADER/Cardinal Health 110, Inc. | 17695563-3765-74cb-e063-6294a90a6120 | 2025-08-07 | Warnings | M005 |
| Antifungal Liquid | TOLNAFTATE | Target Corporation | 1dff278f-47bc-459a-e063-6394a90a2646 | 2025-08-07 | Warnings | M005 |
| Antifungal Liquid | TOLNAFTATE | TopCo Associates | 19c268a1-7b2e-63c9-e063-6394a90acddc | 2025-08-07 | Warnings | M005 |
| Antifungal Liquid Maximum Strength | TOLNAFTATE | Walgreens Company | 137eabb7-cb4f-1631-e063-6294a90ab847 | 2025-08-07 | Warnings | M005 |
| WCTNGO Fungal Nail Treatment Swabs | TOLNAFTATE,UNDECYLENIC ACID | Shenzhen Boyimei Technology Co., Ltd. | 3bad0d73-b33d-b962-e063-6294a90a7ba7 | 2025-08-06 | Warnings | M005 |
| ONIADBA Nail Fungus Treatment Pen | TOLNAFTATE,UNDECYLENIC ACID | Shenzhen Boyimei Technology Co., Ltd. | 3bad19f1-d5b3-c5de-e063-6294a90a0c03 | 2025-08-06 | Warnings | M005 |
| Antifungal Liquid | TOLNAFTATE | Premier Brands of America Inc | 2644ba07-aaee-6402-e063-6394a90a2827 | 2025-08-06 | Warnings | M005 |
| Anti- Fungal Miconazole Nitrate | MICONAZOLE NITRATE | Premier Brands of America Inc. | f186bdc1-db6c-0fab-e053-2995a90a7c58 | 2025-08-06 | Warnings | M005 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 309367 | clotrimazole 1 % Topical Cream | PSN | 4a4b304a-1acc-9185-e063-6394a90a1176 | 1 |
| 309367 | clotrimazole 10 MG/ML Topical Cream | SCD | 4a4b304a-1acc-9185-e063-6394a90a1176 | 1 |
| 309367 | clotrimazole 1 % Topical Cream | SY | 4a4b304a-1acc-9185-e063-6394a90a1176 | 1 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 85248-101-01 | 85248010101 | 30 g in 1 BOTTLE (85248-101-01) | 30 g | 2026-02-08 | No | No | Current |
| 85248-101-02 | 85248010102 | 60 g in 1 BOTTLE (85248-101-02) | 60 g | 2026-02-08 | No | No | Current |