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 |
|---|---|---|---|---|---|---|
| Miconazole Nitrate | ATHLETES FOOT POWDER SPRAY TALC FREE | Chain Drug Marketing Association | 327095bd-a7c9-291d-e063-6394a90afafa | 2026-06-09 | Warnings | M005 |
| Tolnaftate | ANTIFUNGAL LIQUID SPRAY | Chain Drug Marketing Association | 34b5c11f-710f-60e4-e063-6394a90a990d | 2026-06-09 | Warnings | M005 |
| Tolnafate | TOLNAFTATE POWDER SPRAY | Chain Drug Marketing Association | 342affe8-0a4d-6fe6-e063-6394a90a8dad | 2026-06-09 | Warnings | M005 |
| Miconazole Nitrate | ATHLETES FOOT POWDER SPRAY TALC FREE | Chain Drug Marketing Association | edc2da26-ae46-4175-86ed-83e1a65f6d14 | 2026-06-09 | Warnings | M005 |
| Tolnaftate | ANTIFUNGAL LIQUID SPRAY | Chain Drug Marketing Association | aa97d2ca-bcf4-3ee1-e053-2a95a90a748d | 2026-06-09 | Warnings | M005 |
| Tolnafate | TOLNAFTATE POWDER SPRAY | Chain Drug Marketing Association | 1bd8e096-1717-4656-b52c-086d2f56f070 | 2026-06-09 | Warnings | M005 |
| BODYKOO JOCK ITCH Cream | CLOTRIMAZOLE1% JOCK ITCH CREAM | Jiangxi Yudexi Pharmaceutical Co., LTD | 53553b31-81bb-d293-e063-6294a90aa0a5 | 2026-06-09 | Warnings | M005 |
| BODYKOO ATHLETE FOOT Cream | MICONAZOLE NITRATE2% ATHLETE FOOT CREAM | Jiangxi Yudexi Pharmaceutical Co., LTD | 53561903-54fe-f8ec-e063-6294a90a19fe | 2026-06-09 | Warnings | M005 |
| Clotrimazole Cream | CLOTRIMAZOLE USP1% | Aldermed Inc. | 53bdd76b-6290-f1d3-e063-6394a90a9ff1 | 2026-06-08 | Warnings | M005 |
| Miconazole Cream | MICONAZOLE NITRATE | Aldermed Inc. | 4a7fc48a-c103-dc84-e063-6394a90ab80f | 2026-06-08 | Warnings | M005 |
| Antifungal Powder | MICONAZOLE NITRATE | Aldermed Inc. | 60954089-5220-4f4c-8595-b5ee4562562c | 2026-06-08 | Warnings | M005 |
| Jock Itch Powder | MICONAZOLE NITRATE | Walgreens Company | 06d2f36c-8615-af08-e063-6394a90aa424 | 2026-06-05 | Warnings | M005 |
| Miconazole Nitrate 2% | JOCK ITCH SPRAY | Walgreens Company | cf6cbaf4-beba-6fdf-e053-2995a90a76d2 | 2026-06-04 | Warnings | M005 |
| Charmpoo Antifungal Cream | MICONAZOLE NITRATE 2% ANTIFUNGAL CREAM | Jiangxi Yudexi Pharmaceutical Co., LTD | 5368b131-7537-8679-e063-6394a90a6754 | 2026-06-04 | Warnings | M005 |
| Nail Fungus Treatment Pen | UNDECYLENIC ACID, TOLNAFTATE | GUANGZHOU SAWEILAN IMPORT & EXPORT TRADING CO., LTD | 3fe842e1-b3db-c003-e063-6394a90a46b8 | 2026-06-04 | Warnings | M005 |
| Lasolex AC | MICONAZOLE NITRATE 2% ANTIFUNGAL | PureTek Corporation | 52bb4bc1-e88f-f5ea-e063-6394a90ae1e8 | 2026-06-03 | Warnings | M005 |
| Clotrimazole | CLOTRIMAZOLE | Sun Pharmaceutical Industries, Inc. | 13a14d3c-bfce-42b5-8463-4ec69e94774e | 2026-06-03 | Warnings | M005 |
| Kopa Haiku Antifungal Cream | MICONAZOLE NITRATE 2% | Trovina Co. Ltd | 43cbad59-9899-ab3b-e063-6294a90a9e12 | 2026-06-02 | Warnings | M005 |
| Athletes Foot Cream | CLOTRIMAZOLE | Shenzhen Miandou Technology Co.,Ltd. | 53451e74-719e-9499-e063-6394a90a9e5a | 2026-06-02 | Warnings | M005 |
| Lasolex AL | MICONAZOLE NITRATE 2% ANTIFUNGAL | PureTek Corporation | 534df9be-b47a-03a1-e063-6394a90a265a | 2026-06-02 | 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 |