NDC 48433-230
Strong Iodine Solution 700 mg per 1 mL / 1400 mg per 1 mL solution/ drops
On the label: Safecor Health, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Safecor Health, LLC | Woburn, MA, United States | Makes it | Problems found, fixed voluntarilyOct 28, 2025 · 10 inspections, 4 with FDA action |
Recalls
- Oct 19, 2023 · Class II · Safecor Health, LLC
CGMP Deviations: Recall due to the absence of USP CGMP compendial requirements.
Lots: Lot # 21A0073, Exp 11/30/2023; 21A0091, Exp. 12/31/2023; 21A0103, Exp 01/31/2024; 21A0135, Exp 03/31/2024; 22A0011, Exp 06/30/2024; 22A0019, Exp 07/31/2024; 22A0057, Exp 09/30/2024; 22A0083, Exp 11/30/2024; 22A0104, Exp 12/31/2024; 22A0110, Exp 01/31/2025; 22A0150, Exp 03/31/2025; 23A0007, Exp 06/3…
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Iodide Ion and Iodine: every company that makes it
- Form
- solution/ drops, oral
- Strength
- 700 mg per 1 mL / 1400 mg per 1 mL
- Approval
- unapproved drug other
- On the market since
- Sep 20, 2008
- Package NDCs
48433-230-15- Official label
- DailyMed (National Library of Medicine), updated Jan 8, 2025
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