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

Is NDC 10237-0469-25 recalled?

Zicam Cold Remedy Medicated Fruit Drops - Elderberry · 25 BAR, CHEWABLE in 1 BOTTLE (10237-469-25)

Yes — this exact package was recalled

1 FDA recall names the code 10237-0469-25 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
zinc acetate anhydrous, zinc gluconate, and sambucus nigra flowering top
Strength
ZINC ACETATE ANHYDROUS 2 [hp_X]/1; ZINC GLUCONATE 2…
Form
Bar, Chewable · Oral
Labeler
Church & Dwight Co., Inc.
Type
Human OTC Drug
Product code
10237-0469

Recalls naming this package

Class II · Moderate risk

Zicam" Medicated Fruit Drops Elderberry Flavor

Labeling: Label Mix-up: The product in the bottle contains elderberry and the label failed to indicate the inclusion of elderberry as an ingredient.

Ongoing Labeling / mix-up Church & Dwight Co., Inc. NDC 10237-469-25 D-0095-2026

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