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

Is NDC 72288-0388-10 recalled?

basic care no drip nasal · 1 BOTTLE, SPRAY in 1 CARTON (72288-388-10) / 30 mL in 1 BOTTLE, SPRAY

Yes — this exact package was recalled

2 FDA recalls name the code 72288-0388-10 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
Oxymetazoline Hydrochloride
Strength
OXYMETAZOLINE HYDROCHLORIDE .05 g/100mL
Form
Spray, Metered · Nasal
Labeler
Amazon.com Services LLC
Type
Human OTC Drug
Product code
72288-0388

Recalls naming this package

Class II · Moderate risk

Maximum Strength No Drip Nasal Spray

CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.

Terminated cGMP deviation Perrigo Company PLC NDC 72288-388-10 D-0614-2022
Class II · Moderate risk

Maximum Strength No Drip Nasal Spray

CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.

Terminated cGMP deviation Perrigo Company PLC NDC 72288-388-10 D-0613-2022

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