Class II · Moderate risk
Sterile EYE DROPS AC
Lack of Assurance of Sterility
National Drug Code
Is NDC 83324-0190-14 recalled?
Quality Choice Eye Drops Irritation Relief · 1 BOTTLE, DROPPER in 1 BOX (83324-190-14) / 15 mL in 1 BOTTLE, DROPPER
Yes — this exact package was recalled
1 FDA recall names the code 83324-0190-14 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.
1 of these recalls is still ongoing.
- Active ingredient
- Tetrahydrozoline HCl, Zinc sulfate
- Strength
- TETRAHYDROZOLINE HYDROCHLORIDE .05 g/100mL; ZINC SULFATE…
- Form
- Solution/ Drops · Ophthalmic
- Labeler
- Quality Choice
- Type
- Human OTC Drug
- Product code
- 83324-0190
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
- 83324-0029 Quality Choice Lubricant Eye Drops High Performance 1
- 83324-0189 Quality Choice Artificial Tears Lubricant Eye Drops 1
- 83324-0191 Quality Choice Moisturizing Relief Eye Drops 1
Free recall alerts
Know the day your medication is recalled
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