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 |
|---|---|---|---|---|---|---|
| SUNMARK MICONAZOLE NITRATE antifungal | MICONAZOLE NITRATE | Strategic Sourcing Services LLC | 7c15d95a-5b89-4789-8c91-3f61d7ec7707 | 2025-07-30 | Warnings | M005 |
| Antifungal | MICONAZOLE NITRATE | Advanced Rx LLC | e13eb653-3916-444a-ae86-1738c0308b79 | 2025-07-28 | Warnings | M005 |
| Meridian Unwrapped Antibacterial Deodorant | BENZETHONIUM CHLORIDE | Yangzhou Hongshengding Chemical Co.,Ltd. | a2b9570f-312c-4f46-994d-efe057b247aa | 2025-07-28 | Warnings | M005 |
| Meridian Antibacterial Deodorant | BENZETHONIUM CHLORIDE | Yangzhou Hongshengding Chemical Co.,Ltd. | b41b130f-48fd-47d4-a94e-74433ae44de2 | 2025-07-28 | Warnings | M005 |
| Rugby Clotrimazole Antifungal Cream | CLOTRIMAZOLE | Preferred Pharmaceuticals Inc. | bd567e91-7152-4612-83e0-8e8a00c2d2c5 | 2025-07-25 | Warnings | M005 |
| Hongocura | UNDECYLENIC ACID, ZINC UNDECYLENATE | MENPER DISTRIBUTORS, INC. | c69b735e-0ffe-4328-bd9f-3c1ac6798c08 | 2025-07-22 | Warnings | M005 |
| Hongocura Pinceladas | UNDECYLENIC ACID | Menper Distributors, Inc. | 4b9a3a70-d646-47c6-b969-5c4d759d23a4 | 2025-07-22 | Warnings | M005 |
| Hongocura M | UNDECYLENIC ACID | MENPER DISTRIBUTORS, INC. | b4adb7b0-59b4-4b3c-9b0e-1869bb543174 | 2025-07-22 | Warnings | M005 |
| Hongocura S | UNDECYLENIC ACID | MENPER DISTRIBUTORS, INC. | 4a21f371-bfc1-4e66-af16-55b3283872b7 | 2025-07-22 | Warnings | M005 |
| FifthPulse Miconazole Nitrate Cream 1oz | MICONAZOLE NITRATE | Front Pharmaceutical PLC | 3a37a3a8-9d05-926c-e063-6294a90a9ed8 | 2025-07-18 | Warnings | M005 |
| FifthPulse Miconazole Nitrate Cream 4oz | MICONAZOLE NITRATE | Front Pharmaceutical PLC | 3a382b79-dde9-dde0-e063-6294a90a53bb | 2025-07-18 | Warnings | M005 |
| FifthPulse clotrimazole cream 4oz | CLOTRIMAZOLE 1% | Front Pharmaceutical PLC | 3a389093-48f2-29cb-e063-6294a90ada37 | 2025-07-18 | Warnings | M005 |
| PHARMBANNER Tea Tree Oil Antifungal Soap. | TEA TREE OIL ANTIFUNGAL SOAP. | Shenzhen Xinxin Yunhai Technology Co., Ltd. | 3a0860b0-346e-7024-e063-6394a90ace81 | 2025-07-16 | Warnings | M005 |
| TopCare Antifungal | CLOTRIMAZOLE | Topco Associates LLC | 6757eb2a-73e0-4bd0-a332-5713fdf3445d | 2025-07-16 | Warnings | M005 |
| UpandUp Clotrimazole | CLOTRIMAZOLE | Target Corporation | cb2b7d38-9988-493b-9843-56c2f59eed2f | 2025-07-16 | Warnings | M005 |
| Jock Itch | CLOTRIMAZOLE | TARGET Corporation | 1ae551e7-69de-4eef-b4f7-5e1a880e631d | 2025-07-16 | Warnings | M005 |
| Athletes Foot | CLOTRIMAZOLE | FRED'S, INC. | d2d8f44e-2dfa-446b-855e-86e0d6d2d0df | 2025-07-15 | Warnings | M005 |
| Tolnaftate Antifungal | TOLNAFTATE | STRATEGIC SOURCING SERVICES LLC | 97ffb6fd-5670-4783-b805-88fe9e43ca96 | 2025-07-15 | Warnings | M005 |
| Miconazole Nitrate | MICONAZOLE NITRATE | STRATEGIC SOURCING SERVICES LLC | 966a1000-3b08-4f2c-a9f8-568f2524b717 | 2025-07-15 | Warnings | M005 |
| Tolnaftate Antifungal | TOLNAFTATE | Amerisource Bergen | a3c9b783-4a36-46b3-a0dc-0696907eaebb | 2025-07-15 | 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 |