Class II · Moderate risk
Strong Iodine Solution U.S.P.
CGMP Deviations: Recall due to the absence of USP CGMP compendial requirements.
National Drug Code
Is NDC 48433-0230-15 recalled?
Strong Iodine Solution · 14 mL in 1 BOTTLE (48433-230-15)
Yes — this exact package was recalled
1 FDA recall names the code 48433-0230-15 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- Strong Iodine Solution
- Strength
- IODINE 700 mg/mL; POTASSIUM IODIDE 1400 mg/mL
- Form
- Solution/ Drops · Oral
- Labeler
- Safecor Health, LLC
- Type
- Human Prescription Drug
- Product code
- 48433-0230
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 48433-0101 See recall 1
- 48433-0104 See recall 1
- 48433-0106 Calcium Antacid 1
- 48433-0108 See recall 1
- 48433-0129 Aspirin Chewable 1
Free recall alerts
Know the day your medication is recalled
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