SANIFOAM HAND SANITIZER
- Product NDC
- 50536-078
- 11-digit product format
- 505360078
- Labeler code
- 50536
- Product ID
- 50536-078_337be473-a521-8a40-e063-6394a90a7312
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- AMERICAN CHEMICAL AND SANITARY SUPPLY INC
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2014-03-12
- Substance
- ALCOHOL
- Active strength
- 62 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 | Product NDC | Package NDC | Code | Status | Reporting period | Archive | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2024-03-11 06:39 UTC · source 2024-03-08 | excluded product | product | 50536-078 | I | Inactivated by FDA | excluded / ndc_excluded.zip | 1332a3947898… | d4bfe170f9cd… | ||
| 2024-03-11 06:39 UTC · source 2024-03-08 | excluded package | package | 50536-078 | 50536-078-01 | I | Inactivated by FDA | excluded / ndc_excluded.zip | 1332a3947898… | d4bfe170f9cd… |
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
- SANIFOAM HAND SANITIZER
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ALCOHOL | 62 mL/100mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 3K9958V90M | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 581660 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| e1cfa8ff-92e0-4931-98c9-287c8dcd5a99 | Available on FDA.report |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 50536-078-01 | 2024-05-09 | C162847 | 48780-1 | 1030e365-16c8-111a-e063-dadaa90a10e2 | ACCS (as PLD) - SANIFOAM HAND SANITIZER (50536-078) |
| 50536-078-01 | 2024-01-30 | C162847 | 48780-1 | 1030e365-16c8-111a-e063-dadaa90a10e2 | ACCS (as PLD) - SANIFOAM HAND SANITIZER (50536-078) |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50536-078-01 | SANIFOAM HAND SANITIZER | 3785 mL in 1 JUG | GEL | 3785 | 11 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| ALCOHOL | ACTIVE INGREDIENT | 3K9958V90M | SANIFOAM HAND SANITIZER (ALCOHOL) GEL [AMERICAN CHEMICAL AND SANITARY SUPPLY INC] | 5 | |
| ALCOHOL | ACTIVE MOIETY | 3K9958V90M | SANIFOAM HAND SANITIZER (ALCOHOL) GEL [AMERICAN CHEMICAL AND SANITARY SUPPLY INC] | 5 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | SANIFOAM HAND SANITIZER (ALCOHOL) GEL [AMERICAN CHEMICAL AND SANITARY SUPPLY INC] | 5 |
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 |
|---|---|---|---|---|---|---|
| Henry Schein Povidone-Iodine Swabsticks | POVIDONE-IODINE | Henry Schein, Inc. | 5854f241-6cfc-4e5a-ba72-92dd0703f728 | 2023-10-13 | Warnings | M003 |
| DawnMist Alcohol Hand Sanitizer | ALCOHOL | Dukal LLC | a2df96a9-8514-6839-e053-2a95a90a9417 | 2023-10-13 | Warnings | M003 |
| DUKAL STING RELIEF PAD | BENZOCAINE | Dukal LLC | 67c1ddc7-8fde-4431-84cb-f757682d5f3e | 2023-10-13 | Warnings | M003 |
| First Aid Only First Aid/Burn | LIDOCAINE HYDROCHLORIDE, BENZALKONIUM CHLORIDE | Acme United Corporation | 07245b54-b193-178e-e063-6394a90a2581 | 2023-10-09 | Warnings | M003 |
| Hand sanitizer 2oz 2pk original | ETHYL ALCOHOL | Rejoice International Corp. | 06dc1730-216a-8b4d-e063-6294a90a4184 | 2023-10-04 | Warnings | M003 |
| Hand sanitizer 1.8oz with extra clip original | ETHYL ALCOHOL | Zhejiang Guoyao Jingyue Aerosol Co., Ltd. | 06dcf8dc-0831-475e-e063-6394a90a9fef | 2023-10-04 | Warnings | M003 |
| Hand sanitizer 2oz 2pk original | ETHYL ALCOHOL | Zhejiang Guoyao Jingyue Aerosol Co., Ltd. | 06dd2427-097c-b0fa-e063-6294a90a4f82 | 2023-10-04 | Warnings | M003 |
| Hand sanitizer 1.8oz with extra clip original | ETHYL ALCOHOL | Rejoice International Corp. | 06da0cc1-95f2-4f88-e063-6394a90a25ea | 2023-10-03 | Warnings | M003 |
| First Aid Antiseptic Alcohol Pads Isopropyl Alcohol 70 Rite Aid | ISOPROPYL ALCOHOL | Rite Aid Corporation | aa0df5fe-62d1-407d-b8f9-a7fd9473d569 | 2023-10-02 | Warnings | M003 |
| Foaming Instant Hand Sanitizer with Aloe | ETHANOL | MCKESSON MEDICAL-SURGICAL INC. | 5c1f69b7-c8d8-477c-b614-47a3287b0e4c | 2023-06-05 | Warnings | M003 |
| Bactine Max Dry | LIDOCAINE HYDROCHLORIDE | WellSpring Pharmaceutical Corporation | 466404cd-c46a-4944-b1ac-3b3b17f436a1 | 2022-12-27 | Warnings | M003 |
| Povidone-Iodine Pad | POVIDONE-IODINE | Shandong Haiyan Medical Manufacture Co., Ltd. | c9187a07-92d5-15ac-e053-2995a90af4cb | 2022-03-19 | Warnings | M003 |
| Alcohol Prep Pad | ISOPROPYL ALCOHOL | Shandong Haiyan Medical Manufacture Co., Ltd. | 1a117840-22d0-4a88-b1a6-e43162a444ab | 2022-03-19 | Warnings | M003 |
| FIRSTAR BZK Antiseptic Towelette | BENZALKONIUM CHLORIDE | JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD. | 28591a97-9291-48c8-a8e3-c419180331b3 | 2021-07-06 | Warnings | M003 |
| Bactine Max | BENZALKONIUM CHLORIDE AND LIDOCAINE HYDROCHLORIDE | WellSpring Pharmaceutical Corporation | 28e8a311-20a4-45a1-8d5d-ca42b101c275 | 2021-02-24 | Warnings | M003 |
| Hand Sanitizer Lemon 2oz | ALCOHOL | Ningbo Rejoice International | b0a4159a-cb07-4ce6-e053-2995a90a76e7 | 2020-10-02 | Warnings | M003 |
| Sanix Alcohol Hand Rub | ALCOHOL | Topiderm, Inc | a4fbb714-4f20-400a-ab98-f1c8807ce6fc | 2020-03-24 | Warnings | M003 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 581660 | ethanol 62 % Topical Gel | PSN | e1cfa8ff-92e0-4931-98c9-287c8dcd5a99 | 11 |
| 581660 | ethanol 0.62 ML/ML Topical Gel | SCD | e1cfa8ff-92e0-4931-98c9-287c8dcd5a99 | 11 |
| 581660 | ethanol 62 % Topical Gel | SY | e1cfa8ff-92e0-4931-98c9-287c8dcd5a99 | 11 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 50536-078-01 | 50536007801 | 3785 mL in 1 JUG (50536-078-01) | 3785 ml | 2014-03-12 | 0000-00-00 | No | No | Current |