Class II · Moderate risk
TheraTears Extra
Lack of Assurance of Sterility
National Drug Code
Is NDC 58790-0010-30 recalled?
TheraTears Extra · 6 POUCH in 1 CARTON (58790-010-30) / 5 VIAL, SINGLE-USE in 1 POUCH / .6 mL in 1 VIAL, SINGLE-USE
Yes — this exact package was recalled
1 FDA recall names the code 58790-0010-30 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
- Carboxymethylcellulose Sodium, Unspecified
- Strength
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED 2.5 mg/mL
- Form
- Solution/ Drops · Ophthalmic
- Labeler
- Medtech Products INC
- Type
- Human OTC Drug
- Product code
- 58790-0010
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.
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