Lotrimin Daily Prevention
- Product NDC
- 11523-0011
- 11-digit product format
- 115230011
- Labeler code
- 11523
- Product ID
- 11523-0011_48850bbc-9ec2-b7ee-e063-6394a90a9f0d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- tolnaftate
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- Bayer HealthCare LLC.
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-02-14
- Substance
- TOLNAFTATE
- Active strength
- 10 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- 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 | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded product | product | d630ba8d3edf… | 732f749b63fb… | |
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded package | package | 11523-0011-1 | d630ba8d3edf… | 732f749b63fb… |
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded package | package | 11523-0011-2 | d630ba8d3edf… | 732f749b63fb… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded product | product | f5e01cc5f278… | a2eaf40c39c3… | |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 11523-0011-1 | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 11523-0011-2 | f5e01cc5f278… | a2eaf40c39c3… |
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
- Lotrimin Daily Prevention
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| TOLNAFTATE | 10 mg/g |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 06KB629TKV | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 313422 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 9e8f9211-e85d-725a-e053-2995a90a09b3 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| fb7ab793-2c12-4079-b100-a64f73bef25a | Product name | 4 | 20240712 |
| b0cbf770-6cc3-4aa4-9158-755110c2b9f7 | Product name | 2 | 20230717 |
| dc7c5daa-021f-40dd-b00d-63982cb2067a | Product name | 1 | 20230426 |
| 08ffbcbf-26df-b99c-1dab-64fc4cfae89f | Product name | 5 | 20200925 |
| 816b97af-edc5-4060-aff1-b814bdbcad50 | Product name | 1 | 20190415 |
| 7cda52fc-125f-421c-8fea-bc1974370c49 | Product name | 2 | 20180703 |
| 419aab54-5d5a-4146-9453-026d4a9991be | Product name | 2 | 20170525 |
| 08ffbcbf-26df-b99c-1dab-64fc4cfae89f | Product name | 2 | 20160823 |
| 89dac932-b90a-4410-9ab1-84c53e57de25 | Product name | 1 | 20150316 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Related label |
|---|---|---|
| 11523-0011-1 | 2026-01-16 | Lotrimin Daily Prevention Powder UI 1612510 |
| 11523-0011-2 | 2026-01-16 | Lotrimin Daily Prevention Powder UI 1612510 |
| 11523-0011-1 | 2025-07-29 | Lotrimin Daily Prevention Powder UI 1612510 |
| 11523-0011-2 | 2025-07-29 | Lotrimin Daily Prevention Powder UI 1612510 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 11523-0011-1 | Lotrimin Daily Prevention | 90 g in 1 BOTTLE | POWDER | 90 | 7 | |
| 11523-0011-2 | Lotrimin Daily Prevention | 28 g in 1 BOTTLE | POWDER | 28 | 7 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 11523-0011 | LOTRIMIN DAILY PREVENTION (TOLNAFTATE) POWDER [BAYER HEALTHCARE LLC.] | 6 | Current NDC, Legacy NDC, 2 package rows | 20241208_9e8f9211-e85d-725a-e053-2995a90a09b3.zip |
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 |
|---|---|---|---|---|---|---|
| Cura Hongo Antifungal | CLOTRIMAZOLE | Pharmadel LLC | df031309-2778-00cf-e053-2a95a90a5eea | 2025-11-17 | Warnings | M005 |
| CharmTex All in One Antibacterial Shave Gel Body Wash | BENZETHONIUM CHLORIDE | Liufangjing Biotechnology (Yangzhou) Co., Ltd | a7433f39-a8d9-4c78-864d-d7ef193a7daf | 2025-11-16 | Warnings | M005 |
| Mint Blast Foot and Shoe Antifungal | UNDECYLENIC ACID 10% | SANSAR, LLC | f7fcac19-7b72-4b7a-a28e-669a0eebec9c | 2025-11-15 | Warnings | M005 |
| Lavender Foot and Shoe Antifungal | UNDECYLENIC ACID 10% | SANSAR, LLC | 9db58924-a84d-4763-badb-b3aeb46e1ea6 | 2025-11-15 | Warnings | M005 |
| Citrus Detox Foot and Shoe Antifungal | UNDECYLENIC ACID 10% | SANSAR, LLC | 6585c9f5-a6cb-4534-9a61-ecbb6dcb7bdc | 2025-11-15 | Warnings | M005 |
| AlphaTip Nail Repair Pen | NAIL REPAIR PEN | Guangzhou Qiexiran Cosmetics Co., Ltd. | 435c7973-8a67-8f51-e063-6394a90af58f | 2025-11-11 | Warnings | M005 |
| Pharmlitalia Antifungal Medicated Body | TOLNAFTATE | Foshan Sugar Max Cosmetics CO.,Ltd | 399302d2-0da4-4167-8884-b34a9aba8686 | 2025-11-10 | Warnings | M005 |
| PerfectHeal Antifungal | CLOTRIMAZOLE | Zhejiang Dingtai Pharmaceutical Co., Ltd | d9750991-8f10-4d6b-8841-bea022d5ad73 | 2025-11-10 | Warnings | M005 |
| PiYanPing Antifungal | MICONAZOLE NITRATE | Zhejiang Dingtai Pharmaceutical Co., Ltd | 840364aa-d799-4163-a9e8-3f10c18f86ae | 2025-11-10 | Warnings | M005 |
| SKINHEAL ANTIFUNGAL | TOLNAFTATE | Zhejiang Dingtai Pharmaceutical Co., Ltd | 570ee9fb-a495-4a99-9215-0cd1bb2e0290 | 2025-11-10 | Warnings | M005 |
| HUA TUO XIAN GAO ANTIFUNGAL | CLOTRIMAZOLE | MADISON ONE ACME INC | e11c4d87-8dc2-44b1-bf6b-12e7ef4f3d1d | 2025-11-10 | Warnings | M005 |
| Selan Antifungal | SELAN ANTIFUNGAL | Trividia Manufacturing Solutions, Inc | 8c7e51a0-0cd5-4ae3-a904-fad7ac6c1a29 | 2025-11-07 | Warnings | M005 |
| Fortinia Ultra | CLOTRIMAZOLE 1% | The Podiatree Company | 43065a59-fb81-b1c2-e063-6294a90a36e0 | 2025-11-07 | Warnings | M005 |
| MICOCLEAR | CLOTRIMAZOLE ANTIFUNGAL | Rising Pharma Holdings, Inc. | d75b7d3c-3f1c-47e1-8122-4645f56a444e | 2025-11-06 | Warnings | M005 |
| Medline | MICONAZOLE NITRATE | Medline Industries, LP | 1ea444eb-f2f5-8c63-e063-6294a90acac8 | 2025-11-06 | Warnings | M005 |
| Miconazole Nitrate | ANTIFUNGAL POWDER SPRAY | Premier Brands of America Inc. | 38ccf19c-2290-ad99-e063-6394a90a5469 | 2025-11-06 | Warnings | M005 |
| Tolnaftate | ANTIFUNGAL POWDER SPRAY WITH BAKING SODA | Target Corporation | 37792b12-c3dc-558f-e063-6294a90a7e75 | 2025-11-06 | Warnings | M005 |
| Tolnafate | TOLNAFTATE POWDER SPRAY | Topco Associates LLC | 5f8ae9ab-5e34-7a60-e053-2991aa0a9817 | 2025-11-06 | Warnings | M005 |
| Tolnaftate | TOLNAFTATE JOCK ITCH POWDER SPRAY TALC FREE | Topco Associates LLC | 5f8ac6b7-c46c-226c-e053-2991aa0a9606 | 2025-11-06 | Warnings | M005 |
| Tolnaftate | ANTIFUNGAL LIQUID SPRAY | Topco Associates LLC | 3dd0df06-3c74-4c34-a69e-4240945f5fa5 | 2025-11-06 | Warnings | M005 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 313422 | tolnaftate 1 % Topical Powder | PSN | 9e8f9211-e85d-725a-e053-2995a90a09b3 | 7 |
| 313422 | tolnaftate 0.01 MG/MG Topical Powder | SCD | 9e8f9211-e85d-725a-e053-2995a90a09b3 | 7 |
| 313422 | tolnaftate 1 % Topical Powder | SY | 9e8f9211-e85d-725a-e053-2995a90a09b3 | 7 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 11523-0011-1 | 11523001101 | 90 g in 1 BOTTLE (11523-0011-1) | 90 g | 2020-02-14 | 0000-00-00 | No | No | Current |
| 11523-0011-2 | 11523001102 | 28 g in 1 BOTTLE (11523-0011-2) | 28 g | 2022-11-01 | 0000-00-00 | No | No | Current |