NDC 61333-221-01 - Lights Povidone Iodine Swabsticks
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 61333-221
- Requested NDC
- 61333-221-01
- Package NDCs from labels
- 61333-221-01, 61333-221-02, 61333-221-03, 61333-221-04, 61333-221-06, 61333-221-05
- Manufacturer
- Lights Medical Manufacture Co., Ltd.
- Effective date
- 2026-07-22
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| 61333-221 Lights Povidone Iodine Swabsticks | Lights Medical Manufacture Co., Ltd. | 2026-07-22 | HUMAN OTC DRUG LABEL |
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 |
|---|---|---|---|---|---|---|
| BD E-Z SCRUB | POVIDONE-IODINE | Becton Dickinson and Company | bc23c292-80cd-4211-b627-2e9984a94526 | 2025-12-08 | Warnings | 85H0HZU99M |
| Hand Sanitizer | HAND SANITIZER | Zhejiang Meimi Technology Co., Ltd. | bf399508-bd29-0d90-e053-2995a90a067f | 2025-12-06 | Warnings | M003 |
| Hand Sanitizer | HAND SANITIZER | Zhejiang Meimi Technology Co., Ltd. | dceb351a-06fb-8222-e053-2a95a90aadbf | 2025-12-06 | Warnings | M003 |
| Hand Sanitizer | HAND SANITIZER | Zhejiang Meimi Technology Co., Ltd. | dcead234-bb98-1ee8-e053-2a95a90a3186 | 2025-12-06 | Warnings | M003 |
| 75% Alcohol Disinfectant | ALCOHOL | Zhejiang Meimi Technology Co., Ltd. | acfdfa78-69e7-27dc-e053-2a95a90a8548 | 2025-12-06 | Warnings | M003 |
| 75% Alcohol Disinfectant | ALCOHOL | Zhejiang Meimi Technology Co., Ltd. | ad0cdcf1-7d8b-dcc9-e053-2995a90a4b4b | 2025-12-06 | Warnings | M003 |
| Hand Sanitizer | HAND SANITIZER | Zhejiang Meimi Technology Co., Ltd. | dceb9358-663c-3c70-e053-2995a90a3524 | 2025-12-06 | Warnings | M003 |
| Hand Sanitizer | HAND SANITIZER | Zhejiang Meimi Technology Co., Ltd. | dced08e7-a0bc-1328-e053-2995a90afb26 | 2025-12-06 | Warnings | M003 |
| Hand Sanitizer | HAND SANITIZER | Zhejiang Meimi Technology Co., Ltd. | dcec13da-586c-6e7e-e053-2a95a90a6cd1 | 2025-12-06 | Warnings | M003 |
| Hand Sanitizer | HAND SANITIZER | Zhejiang Meimi Technology Co., Ltd. | dceced03-eeb8-fced-e053-2995a90afd5c | 2025-12-06 | Warnings | M003 |
| Hand Sanitizer | HAND SANITIZER | Zhejiang Meimi Technology Co., Ltd. | dced643b-96fb-193f-e053-2a95a90a16aa | 2025-12-06 | Warnings | M003 |
| Betadine Foam Cleanser | BENZALKONIUM CHLORIDE | Atlantis Consumer Healthcare, Inc. | 3be9fa6e-3ae8-496b-876b-f81f1cd98af4 | 2025-12-05 | Warnings | M003 |
| 2XL Mega Rolls Sanitizing Wipes | BENZALKONIUM CHLORIDE | 2xl Corporation | 9da541ab-6836-4149-a86d-3b2f2e586628 | 2025-12-05 | Warnings | M003 |
| Hand Wipes | BENZALKONIUM CHLORIDE | Advanced Ultrasound Solutions Inc. | 2c2abaa8-c152-470b-a4d9-5056815a1987 | 2025-12-05 | Warnings | M003 |
| Benzalkonium Chloride | SANITIZING HAND WIPES | ALO NEW YORK LLC | d3d95355-3af7-43e3-e053-2a95a90a0fa4 | 2025-12-05 | Warnings | M003 |
| Giant Eagle Antibacterial Hand Wipes | BENZALKONIUM CHLORIDE | Giant Eagle | e20e9a93-03c3-77f8-e053-2995a90ae59f | 2025-12-05 | Warnings | M003 |
| Antibacterial Wipes | BENZALKONIUM CHLORIDE | ERC Acquisition, Inc | dc6c39af-447c-481a-98b5-33b8f09b83bc | 2025-12-05 | Warnings | M003 |
| Sanitex Antibacterial Hand Wipes Fresh Scent | BENZALKONIUM CHLORIDE | Precare Corp | 48907146-ca66-46e1-928b-a8f968a6bff8 | 2025-12-05 | Warnings | M003 |
| Benzalkonium Chloride | ANTIBACTERIAL HAND WIPES | Quest USA Corp | d9ab219d-07e3-2019-e053-2a95a90a1668 | 2025-12-05 | Warnings | M003 |
| Benzalkonium Chloride | DUAL ACTION ANTIBACTERIAL WIPES | Avro Enterprises LLC | cf42e470-19c8-2e11-e053-2995a90ae90d | 2025-12-05 | Warnings | M003 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.