Lotrimin Daily Prevention Deo
- Product NDC
- 11523-0010
- 11-digit product format
- 115230010
- Labeler code
- 11523
- Product ID
- 11523-0010_4526ca36-993e-b574-e063-6294a90a8fba
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Tolnaftate
- Dosage form
- AEROSOL, 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
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 Deo
- 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 |
|---|---|
| 705934 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 9e8bfb78-ad81-93d0-e053-2995a90aa41d | Available on FDA.report |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 11523-0010-1 | Lotrimin Daily Prevention Deo | 160 g in 1 CAN | AEROSOL, POWDER | 160 | 10 | |
| 11523-0010-2 | Lotrimin Daily Prevention Deo | 133 g in 1 CAN | AEROSOL, POWDER | 133 | 10 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 11523-0010 | LOTRIMIN DAILY PREVENTION DEO (TOLNAFTATE) AEROSOL, POWDER [BAYER HEALTHCARE LLC.] | 9 | Current NDC, Legacy NDC, 2 package rows | 20241208_9e8bfb78-ad81-93d0-e053-2995a90aa41d.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 |
|---|---|---|---|---|---|---|
| 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 |
|---|---|---|---|---|
| 705934 | tolnaftate 1 % Powder Spray | PSN | 9e8bfb78-ad81-93d0-e053-2995a90aa41d | 10 |
| 705934 | tolnaftate 0.01 MG/MG Powder Spray | SCD | 9e8bfb78-ad81-93d0-e053-2995a90aa41d | 10 |
| 705934 | tolnaftate 1 % Powder Spray | SY | 9e8bfb78-ad81-93d0-e053-2995a90aa41d | 10 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 11523-0010-1 | 11523001001 | 160 g in 1 CAN (11523-0010-1) | 160 g | 2020-02-14 | 0000-00-00 | No | No | Current |
| 11523-0010-2 | 11523001002 | 133 g in 1 CAN (11523-0010-2) | 133 g | 2020-02-14 | 0000-00-00 | No | No | Current |