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 |
|---|---|---|---|---|---|---|
| Anti-Fungal Powder | MICONAZOLE NITRATE | TopCo Associates | 19c3fbc5-abde-57df-e063-6394a90a125c | 2025-11-06 | Warnings | M005 |
| Tolnaftate | FOOT ODOR CONTROL SPRAY | Topco Associates LLC | 17993a9f-0d44-43a1-8608-94ee8a08b539 | 2025-11-06 | Warnings | M005 |
| DVO Estriol cream | ESTRIOL0.2% | Guangzhou Huixue Biotechnology Co., Ltd. | 42e4cc84-7c00-6937-e063-6294a90a0c09 | 2025-11-05 | Warnings | M005 |
| Medline | MICONAZOL NITRATE | Medline Industries, LP | dad58efb-cc20-577a-e053-2a95a90abd9d | 2025-11-03 | Warnings | M005 |
| Tolnafate | TOLNAFTATE POWDER SPRAY | HEB | c6af941a-0b85-4611-a6f3-b13fcf3c4a87 | 2025-11-03 | Warnings | M005 |
| Tolnaftate | FOOT ODOR CONTROL SPRAY | HEB | c585605b-ecb8-4dd8-9205-a9be02d751fa | 2025-11-03 | Warnings | M005 |
| Premier Solutions Antifungal Tolnaftate Liquid | TOLNAFTATE | Premier Brands of America, Inc. | e1971c1c-5687-577b-e053-2a95a90ad95f | 2025-11-03 | Warnings | M005 |
| Miconazole nitrate | ANTIFUNGAL MICONAZOLE LIQUID CONTINUOUS SPRAY | Premier Brands of America Inc. | 3803c643-35d1-06d4-e063-6294a90ac6f6 | 2025-11-03 | Warnings | M005 |
| Anti-fungal Powder Miconazole Nitrate | MICONAZOLE NITRATE | Meijer Distribution Inc | 03fd069d-685d-b8ac-e063-6394a90a31f8 | 2025-10-31 | Warnings | M005 |
| Tolnaftate | ANTIFUNGAL LIQUID SPRAY | Premier Brands of America Inc. | 7a6a63cd-e87d-4229-8acf-b65d63909eb6 | 2025-10-31 | Warnings | M005 |
| Azolen | MICONAZOLE NITRATE | Stratus Pharmaceuticals, Inc. | 9c2574f3-3be4-405a-9c87-943dc6ef8777 | 2025-10-30 | Warnings | M005 |
| Family Care Antifungal | CLOTRIMAZOLE | United Exchange Corp. | 63255079-ecf1-1e77-e053-2a91aa0a7b6c | 2025-10-30 | Warnings | M005 |
| Miconazorb AF | MICONAZOLE NITRATE | AmerisourceBergen Drug Corporation | 13a20d21-42d5-fe56-e063-6394a90aaf57 | 2025-10-30 | Warnings | M005 |
| Antifungal Liquid Continuous | MICONAZOLE NITRATE | Family Dollar Services, Inc | 17cc4601-f946-df8b-e063-6394a90a3897 | 2025-10-30 | Warnings | M005 |
| Tolnaftate | ANTIFUNGAL LIQUID SPRAY | ARMY & AIR FORCE EXCHANGE SERVICE | 932b1be8-3dbb-49ae-822a-c44a24fbe36a | 2025-10-30 | Warnings | M005 |
| Miconazole nitrate | ANTIFUNGAL MICONAZOLE LIQUID CONTINUOUS SPRAY | GEISS, DESTIN AND DUNN, INC. | c367c2e8-5423-bf01-e053-2a95a90ab8e9 | 2025-10-30 | Warnings | M005 |
| Miconazole Nitrate | JOCK ITCH SPRAY | Harris Teeter, LLC | 636b0d6f-4e36-4c96-9e71-7bfdebb7f3cb | 2025-10-30 | Warnings | M005 |
| Tolnaftate | ANTIFUNGAL LIQUID SPRAY | Harris Teeter, LLC | f140e9bb-507b-4048-8b7b-8cc51b6a497d | 2025-10-30 | Warnings | M005 |
| HEB Athlete Foot Antifungal | MICONAZOLE NITRATE | HEB | 2e204111-b5d3-0220-e063-6294a90a67bb | 2025-10-30 | Warnings | M005 |
| Tolnaftate | ANTIFUNGAL SPRAY LIQUID | Kroger Co. | 0cfebac3-684d-4599-b75f-9a82708db717 | 2025-10-30 | 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 |