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 |
|---|---|---|---|---|---|---|
| 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 |
|---|---|---|---|---|
| 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 |