Azolen
- Product NDC
- 58980-818
- 11-digit product format
- 589800818
- Labeler code
- 58980
- Product ID
- 58980-818_0892f504-c8a8-4aff-9901-223635b876c2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Miconazole Nitrate
- Dosage form
- TINCTURE
- Route
- TOPICAL
- Labeler
- Stratus Pharmaceuticals, Inc.
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2017-09-15
- Substance
- MICONAZOLE NITRATE
- Active strength
- 20 mg/mL
- Pharmacologic classes
- Azole Antifungal [EPC], Azoles [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- 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
- Azolen
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| MICONAZOLE NITRATE | 20 mg/mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| VW4H1CYW1K | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 998525 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 9c2574f3-3be4-405a-9c87-943dc6ef8777 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 48747306-602a-42cc-957b-5b0c69158eee | Product name | 1 | 20180604 |
| 3a55f4fb-5aec-4c88-0ff7-4d608ad4866a | Product name | 1 | 20140508 |
| 5b9a7965-36d2-8412-dcaf-f76a65411611 | Product name | 1 | 20140508 |
| db5ebcdb-b6ae-21cd-4dc5-76cd84b5578b | Product name | 1 | 20140508 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 58980-818-10 | Azolen | 29.57 mL in 1 BOTTLE, WITH APPLICATOR | TINCTURE | 29.57 | 4 | |
| 58980-818-10 | Azolen | 1 in 1 BOX | TINCTURE | 1 | 4 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 58980-818-10 | ML - Milliliter | 58980-818 | 5725ebf8-1f7d-4134-bb0d-aa43535c4da2 | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| Miconazole Nitrate | ACTIVE INGREDIENT | VW4H1CYW1K | AZOLEN (MICONAZOLE NITRATE) TINCTURE [STRATUS PHARMACEUTICALS, INC.] | 2 | |
| Miconazole | ACTIVE MOIETY | 7NNO0D7S5M | AZOLEN (MICONAZOLE NITRATE) TINCTURE [STRATUS PHARMACEUTICALS, INC.] | 2 | |
| Acetic Acid | INACTIVE INGREDIENT | Q40Q9N063P | AZOLEN (MICONAZOLE NITRATE) TINCTURE [STRATUS PHARMACEUTICALS, INC.] | 2 | |
| Benzyl Alcohol | INACTIVE INGREDIENT | LKG8494WBH | AZOLEN (MICONAZOLE NITRATE) TINCTURE [STRATUS PHARMACEUTICALS, INC.] | 2 | |
| Isopropyl Alcohol | INACTIVE INGREDIENT | ND2M416302 | AZOLEN (MICONAZOLE NITRATE) TINCTURE [STRATUS PHARMACEUTICALS, INC.] | 2 | |
| Laureth-4 | INACTIVE INGREDIENT | 6HQ855798J | AZOLEN (MICONAZOLE NITRATE) TINCTURE [STRATUS PHARMACEUTICALS, INC.] | 2 | |
| Sodium Hydroxide | INACTIVE INGREDIENT | 55X04QC32I | AZOLEN (MICONAZOLE NITRATE) TINCTURE [STRATUS PHARMACEUTICALS, INC.] | 2 | |
| Water | INACTIVE INGREDIENT | 059QF0KO0R | AZOLEN (MICONAZOLE NITRATE) TINCTURE [STRATUS PHARMACEUTICALS, INC.] | 2 |
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 |
|---|---|---|---|---|
| 998525 | miconazole nitrate 2 % Topical Solution | PSN | 9c2574f3-3be4-405a-9c87-943dc6ef8777 | 4 |
| 998525 | miconazole nitrate 20 MG/ML Topical Solution | SCD | 9c2574f3-3be4-405a-9c87-943dc6ef8777 | 4 |
| 998525 | miconazole nitrate 2 % Topical Solution | SY | 9c2574f3-3be4-405a-9c87-943dc6ef8777 | 4 |
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 58980-818-10 | 58980081810 | 1 BOTTLE, WITH APPLICATOR in 1 BOX (58980-818-10) / 29.57 mL in 1 BOTTLE, WITH APPLICATOR | 2017-09-15 | 0000-00-00 | No | No | Current |