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

Is NDC 0363-3233-15 recalled?

Walgreens Earache Drops · 1 BOTTLE, DROPPER in 1 CARTON (0363-3233-15) / 10 mL in 1 BOTTLE, DROPPER

Yes — this exact package was recalled

1 FDA recall names the code 0363-3233-15 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
belladonna leaf, calcium carbonate, chamomile, lycopodium clavatum spore, anemone patens, and sulfur
Strength
BELLADONNA LEAF 30 [hp_C]/mL; CALCIUM CARBONATE 30…
Form
Liquid · Auricular (otic)
Labeler
Walgreen Company
Type
Human OTC Drug
Product code
0363-3233

Recalls naming this package

Class II · Moderate risk

Earache Drops

Microbial contamination of non-sterile product.

Terminated Microbial contamination Grato Holdings, Inc. NDC 0363-3233-15 D-0991-2022

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