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

Is NDC 51801-0004-40 recalled?

GloStrips · 100 POUCH in 1 CARTON (51801-004-40) / 1 STRIP in 1 POUCH

Yes — this exact package was recalled

1 FDA recall names the code 51801-0004-40 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
Rose Bengal Sodium
Strength
ROSE BENGAL SODIUM 1.3 mg/1
Form
Strip · Ophthalmic
Labeler
Nomax Inc.
Type
Human Prescription Drug
Product code
51801-0004

Recalls naming this package

Class III ยท Low risk

Rose Bengal GloStrips

Failed Content Uniformity Specifications: The product may not meet finished product release specifications, including the uniformity of dosage due to a packaging degradation related to the adhesive component of the paper pouch that can impact the level of rose bengal present in the strips.

Terminated Wrong potency / content Nomax Inc NDC 51801-004-01 D-0962-2015

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