meijer
- Product NDC
- 41250-305
- 11-digit product format
- 412500305
- Labeler code
- 41250
- Product ID
- 41250-305_38f991cb-365d-1ce2-e063-6394a90ace1d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Clotrimazole
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Meijer Distribution Inc
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 1993-08-31
- Substance
- CLOTRIMAZOLE
- Active strength
- 10 mg/g
- Pharmacologic classes
- Azole Antifungal [EPC], Azoles [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Package NDC | Code | Status | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded product | product | U | Excluded because listing certification expired | 302b2466d912… | e7b80fea0513… | |
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded package | package | 41250-305-03 | U | Excluded because listing certification expired | 302b2466d912… | e7b80fea0513… |
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded package | package | 41250-305-02 | U | Excluded because listing certification expired | 302b2466d912… | e7b80fea0513… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded product | product | U | Excluded because listing certification expired | ed331223b511… | 672a5bd82f5f… | |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded package | package | 41250-305-03 | U | Excluded because listing certification expired | ed331223b511… | 672a5bd82f5f… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded package | package | 41250-305-02 | U | Excluded because listing certification expired | ed331223b511… | 672a5bd82f5f… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded product | product | U | Excluded because listing certification expired | 0efc9e666f02… | f202fb6c5f17… | |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded package | package | 41250-305-03 | U | Excluded because listing certification expired | 0efc9e666f02… | f202fb6c5f17… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded package | package | 41250-305-02 | U | Excluded because listing certification expired | 0efc9e666f02… | f202fb6c5f17… |
| 2022-08-30 03:57 UTC · source 2022-08-29 | excluded product | product | I | Inactivated by FDA | fb8cb913e6d1… | eb8c232b6be0… | |
| 2022-08-30 03:57 UTC · source 2022-08-29 | excluded package | package | 41250-305-02 | I | Inactivated by FDA | fb8cb913e6d1… | eb8c232b6be0… |
| 2022-04-09 23:13 UTC · source 2022-04-08 | excluded product | product | I | Inactivated by FDA | 86f5da6cb304… | a595104c45d7… | |
| 2022-04-09 23:13 UTC · source 2022-04-08 | excluded package | package | 41250-305-02 | I | Inactivated by FDA | 86f5da6cb304… | a595104c45d7… |
| 2022-04-04 05:40 UTC · source 2022-04-01 | excluded product | product | I | Inactivated by FDA | bd6a592717d7… | 303034d00443… | |
| 2022-04-04 05:40 UTC · source 2022-04-01 | excluded package | package | 41250-305-02 | I | Inactivated by FDA | bd6a592717d7… | 303034d00443… |
| 2021-12-27 23:28 UTC · source 2021-12-27 | excluded product | product | I | Inactivated by FDA | 8dfbde2a14a4… | c9ff85d89658… | |
| 2021-12-27 23:28 UTC · source 2021-12-27 | excluded package | package | 41250-305-02 | I | Inactivated by FDA | 8dfbde2a14a4… | c9ff85d89658… |
| 2020-12-18 03:04 UTC · source 2020-12-17 | excluded product | product | I | Inactivated by FDA | e2bbac7714bc… | 27bdfed8d636… | |
| 2020-12-18 03:04 UTC · source 2020-12-17 | excluded package | package | 41250-305-02 | I | Inactivated by FDA | e2bbac7714bc… | 27bdfed8d636… |
| 2020-06-10 20:45 UTC · source 2020-06-10 | excluded product | product | I | Inactivated by FDA | 9bebd1f3094a… | 5416666fcb17… | |
| 2020-06-10 20:45 UTC · source 2020-06-10 | excluded package | package | 41250-305-02 | I | Inactivated by FDA | 9bebd1f3094a… | 5416666fcb17… |
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
- meijer
- Brand name suffix
- Athletes Foot
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| CLOTRIMAZOLE | 10 mg/g |
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 |
|---|---|
| fdb15cd8-6726-4150-9b9d-6ef3ee01a5d2 | 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 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Related label |
|---|---|---|
| 41250-305-02 | 2025-02-11 | meijer ™ Athlete's Foot |
| 41250-305-03 | 2025-02-11 | meijer ™ Athlete's Foot |
| 41250-305-02 | 2025-01-30 | meijer ™ Athlete's Foot |
| 41250-305-03 | 2025-01-30 | meijer ™ Athlete's Foot |
| 41250-305-02 | 2023-12-01 | meijer ™ Athlete's Foot |
| 41250-305-02 | 2020-01-31 | meijer ™ Athlete's Foot |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 41250-305-02 | meijerAthletes Foot | 1 in 1 CARTON | CREAM | 1 | 6 | |
| 41250-305-02 | meijerAthletes Foot | 30 g in 1 TUBE | CREAM | 30 | 6 | |
| 41250-305-03 | meijerAthletes Foot | 30 g in 1 TUBE | CREAM | 30 | 6 | |
| 41250-305-03 | meijerAthletes Foot | 1 in 1 CARTON | CREAM | 1 | 6 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
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 |
|---|---|---|---|---|---|---|
| Evercare Antifungal Treatment Super Absorbent Powder | MICONAZOLE NITRATE | PANEFFORT, LLC | f91910f3-b461-43a4-9120-fda69483fffa | 2023-10-26 | Warnings | M005 |
| Thera plus Antifungal Clotrimazole | CLOTRIMAZOLE | FOURSTAR GROUP USA, INC. | 1265be99-8922-4b76-bd63-19bfb42c3896 | 2023-10-26 | Warnings | M005 |
| Thera plus Antifungal Tolnaftate | TOLNAFTATE | FOURSTAR GROUP USA, INC. | c628dda8-7a6d-5f3a-e053-2995a90a35f8 | 2023-10-26 | Warnings | M005 |
| Povidone Iodine | POVIDONE IODINE | Jianerkang Medical Co., Ltd | e1789944-3a41-4c86-b173-3a6993ae2141 | 2023-10-23 | Warnings | M005 |
| Povidone Iodine Impregnated | POVIDONE IODINE | Jianerkang Medical Co., Ltd | 14f2a1dd-92c2-49e8-9fa0-a9d88e8c530d | 2023-10-23 | Warnings | M005 |
| Povidone Iodine Impregnated | POVIDONE IODINE | Jianerkang Medical Co., Ltd | b82cea56-b09f-411d-a6cf-c53b3ce0e3b6 | 2023-10-23 | Warnings | M005 |
| Povidone Iodine Scrub | POVIDONE-IODINE | Jianerkang Medical Co., Ltd | 78131b57-1ffc-4eb8-821e-f7bb73300fe9 | 2023-10-23 | Warnings | M005 |
| Povidone Iodine | POVIDONE IODINE | Jianerkang Medical Co., Ltd | eb30e5de-9074-4760-8e92-e1d1c127227d | 2023-10-23 | Warnings | M005 |
| Povidone Iodine | POVIDONE IODINE | Jianerkang Medical Co., Ltd | 0bd3de76-b726-41f1-87bc-14ab8a1eca8e | 2023-10-23 | Warnings | M005 |
| Povidone Iodine Prep Pad | POVIDONE-IODINE | Jianerkang Medical Co., Ltd | be85ec5b-eb49-4f1a-a87d-5c9705a20f23 | 2023-10-22 | Warnings | M005 |
| EVERLIT CARE Hand Sanitizer | ETHYL ALCOHOL | Nantong Health & Beyond Hygienic Products Inc. | 579c1ab5-50b4-4b5a-a189-c1e2827d0c3a | 2023-10-14 | Warnings | M005 |
| Micomitin Antifungal | CLOTRIMAZOLE | PureTek Corporation | dd05f5f9-2412-1295-e053-2995a90acb96 | 2022-02-14 | Warnings | M005 |
| Micatin | MICONAZOLE NITRATE | WellSpring Pharmaceutical Corporation | 96c56ba1-c3a8-48ce-ab58-550959485e3c | 2016-04-07 | Warnings | M005 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 309367 | clotrimazole 1 % Topical Cream | PSN | fdb15cd8-6726-4150-9b9d-6ef3ee01a5d2 | 6 |
| 309367 | clotrimazole 10 MG/ML Topical Cream | SCD | fdb15cd8-6726-4150-9b9d-6ef3ee01a5d2 | 6 |
| 309367 | clotrimazole 1 % Topical Cream | SY | fdb15cd8-6726-4150-9b9d-6ef3ee01a5d2 | 6 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 41250-305-02 | 41250030502 | 1 TUBE in 1 CARTON (41250-305-02) / 30 g in 1 TUBE | 1 tube | 1993-08-31 | No | No | Current |
| 41250-305-03 | 41250030503 | 1 TUBE in 1 CARTON (41250-305-03) / 30 g in 1 TUBE | 1 tube | 2023-12-15 | No | No | Current |