AWAS ALCOHOLSPRAY
- Product NDC
- 77039-024
- 11-digit product format
- 770390024
- Labeler code
- 77039
- Product ID
- 77039-024_2cf6b8fa-ee81-3e75-e063-6294a90a7350
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- alcohol
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- IDO PHARM
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-08-16
- Substance
- ALCOHOL
- Active strength
- 83 mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- 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 |
|---|---|---|---|---|---|
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded product | product | 302b2466d912… | e7b80fea0513… | |
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded package | package | 77039-024-01 | 302b2466d912… | e7b80fea0513… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded product | product | ed331223b511… | 672a5bd82f5f… | |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded package | package | 77039-024-01 | ed331223b511… | 672a5bd82f5f… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded product | product | 0efc9e666f02… | f202fb6c5f17… | |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded package | package | 77039-024-01 | 0efc9e666f02… | f202fb6c5f17… |
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
- AWAS ALCOHOLSPRAY
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ALCOHOL | 83 mL/100mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 3K9958V90M | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 2288438 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 03010837-0289-3e08-e063-6394a90a7d04 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 3c386306-c48a-413e-bb69-70cb268496f3 | Product name | 1 | 20210727 |
| 7792dadb-52b6-46b6-8fdf-80b1171065b5 | Product name | 1 | 20180810 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 77039-024-01 | 2025-02-03 | C162847 | 48780-1 | 2cef2736-92ac-d83d-e063-dadaa90ab31f | 03010837-0289-3e08-e063-6394a90a7d04 |
| 77039-024-01 | 2025-01-30 | C162847 | 48780-1 | 2cef2736-92ac-d83d-e063-dadaa90ab31f | 03010837-0289-3e08-e063-6394a90a7d04 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 77039-024-01 | AWAS ALCOHOLSPRAY | 500 mL in 1 BOTTLE, SPRAY | SPRAY | 500 | 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 |
|---|---|---|---|---|---|---|
| Tolnaftate | TOLNAFTATE | Sheffield Pharmaceuticals LLC | ca52af37-c3a2-414c-a24a-a37a92925133 | 2025-02-20 | Warnings | M005 |
| Dr Sheffield Athletes Foot | CLOTRIMAZOLE | Sheffield Pharmaceuticals LLC | b8b8e6b2-1022-4592-91ba-3cf94c7cf318 | 2025-02-19 | Warnings | M005 |
| UKVOA Toenail Fungus Treatment | TOLNAFTATE 1% FUNGI NAIL | Jiashen International Trade Limited | 2e3cde7b-850e-f9d2-e063-6394a90adb18 | 2025-02-16 | Warnings | M005 |
| UKOVA FOOT ODOR PROBIOTIC | TOLNAFTATE 1% FUNGI NAIL | Jiashen International Trade Limited | 2de0225d-dd85-e2da-e063-6294a90a050b | 2025-02-11 | Warnings | M005 |
| Dr. Scholls Instant Cool Athletes Foot Wipes | TOLNAFTATE | Cosco International, Inc. | cde656a9-7841-4a73-a2f4-f5a76a3e15c1 | 2025-02-06 | Warnings | M005 |
| Silka Athletes Foot | MICONAZOLE NITRATE | Genomma Lab USA | 307104a2-2df6-43b0-bf3f-f4d93d3e40f1 | 2025-02-05 | Warnings | M005 |
| MICONAZOLE Nitrate | MICONAZOLE NITRATE | NuCare Pharmaceuticals,Inc. | fd7dd2eb-03a7-ef1f-e053-6294a90a8557 | 2025-02-04 | Warnings | M005 |
| Molecular AF | TOLNAFTATE | Renu Laboratories, LLC | 1b47e687-29cf-48ce-8bc3-ac8f44f05baa | 2025-02-03 | Warnings | M005 |
| Dermatool Fungal Nail Treatment | TOLNAFTATE 1% | Papalo Group LLC | 2d2c0e12-123d-75bd-e063-6394a90ae546 | 2025-01-31 | Warnings | M005 |
| 70% Isopropyl Alcohol | ISOPROPYL ALCOHOL | IDO PHARM | d5833c6f-81dd-6ff6-e053-2995a90ac76d | 2025-01-30 | Warnings | M005 |
| AWAS ALCOHOLSPRAY | ALCOHOL | IDO PHARM | 03010837-0289-3e08-e063-6394a90a7d04 | 2025-01-30 | Warnings | M005 77039-024 |
| ELON Dual Defense Anti Fungal Formula | UNDECYLENIC ACID | Little Giant Holdings LLC | 45c4567d-7876-6459-e054-00144ff88e88 | 2025-01-28 | Warnings | M005 |
| DCH Labs Antifungal Jock | MICONAZOLE NITRATE 2% | Derma Care Research Labs, LLC | fc749882-2e1e-cad3-e053-6294a90a33ca | 2025-01-27 | Warnings | M005 |
| Antifungal Pen | UNDECYLENIC ACID 25% | XF Agencija Limited | a15d4512-0fc6-424f-9dd3-ab433d9b7a26 | 2025-01-27 | Warnings | M005 |
| Mata Hongos | UNDECYLENIC ACID | Vitamex USA, Corp | 21ca7edb-dde3-5846-e063-6394a90a3cc0 | 2025-01-23 | Warnings | M005 |
| Povidone Iodine Scrub | POVIDONE-IODINE | Jianerkang Medical Co., Ltd | 53cb4c0d-40b5-4cf3-b122-fd6dd654883f | 2025-01-23 | Warnings | M005 |
| NATUREPLEX TOLNAFTATE ANTIFUNGAL | TOLNAFTATE | Natureplex, LLC | 575b8645-9166-4242-a74f-f4aa4acaaf3d | 2025-01-15 | Warnings | M005 |
| Tobcharm Antifungal Treatment Cream | ANTIFUNGAL TREATMENT CREAM | Guangzhou Zanming Trading Co., Ltd. | 2ba241cc-2767-1190-e063-6294a90ac66b | 2025-01-13 | Warnings | M005 |
| MICONAZOLE Nitrate 2% | MICONAZOLE NITRATE | Akron Pharma Inc. | 8933f939-098a-4257-8d9c-4d5c3240e9a6 | 2025-01-10 | Warnings | M005 |
| ANTI-ITCH FEMININE CARE | HYDROCORTISONE 0.5% | OL PHARMA TECH, LLC Drs PHARMACY | d6fa5ff3-ebdc-222d-e053-2a95a90a88d5 | 2025-01-09 | Warnings | M005 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 2288438 | ethanol 83 % Topical Spray | PSN | 03010837-0289-3e08-e063-6394a90a7d04 | 2 |
| 2288438 | ethanol 0.83 ML/ML Topical Spray | SCD | 03010837-0289-3e08-e063-6394a90a7d04 | 2 |
| 2288438 | ethanol 83 % Topical Spray | SY | 03010837-0289-3e08-e063-6394a90a7d04 | 2 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 77039-024-01 | 77039002401 | 500 mL in 1 BOTTLE, SPRAY (77039-024-01) | 500 ml | 2023-08-16 | No | No | Current |