Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 70677-1158-01 recalled?

Foster and Thrive Advanced Relief Eye Drops · 1 BOTTLE, DROPPER in 1 BOX (70677-1158-1) / 15 mL in 1 BOTTLE, DROPPER

Yes — this exact package was recalled

2 FDA recalls name the code 70677-1158-01 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.

2 of these recalls are still ongoing.

Active ingredient
Polyethylene glycol 400, Tetrahydrozoline HCl
Strength
TETRAHYDROZOLINE HYDROCHLORIDE .05 g/100mL; POLYETHYLENE…
Form
Solution/ Drops · Ophthalmic
Labeler
Strategic Sourcing Services LLC
Type
Human OTC Drug
Product code
70677-1158

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