National Drug Code

Is NDC 0363-6171-09 recalled?

Q: Is NDC 0363-6171-09 recalled?

Yes - this exact package was recalled. 1 FDA recall(s) name this product; 0 still ongoing. A recall usually applies to specific lots - check the lot number on your package and ask your pharmacist.

Sinus Pressure, Pain and Cough · 2 BLISTER PACK in 1 CARTON (0363-6171-09) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Yes — this exact package was recalled

1 FDA recall names the code 0363-6171-09 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: Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl
Strength: ACETAMINOPHEN 325 mg/1; DEXTROMETHORPHAN HYDROBROMIDE 10…
Form: Tablet, Film Coated · Oral
Labeler: Walgreen Company
Type: Human OTC Drug
Product code: 0363-6171

Recalls naming this package

Oct 11, 2022 Class III · Low risk

NDC 0363-6171-09 Walgreens Sinus Pressure

Boxes mislabeled to read "Decongestant Free", but the product contains Phenylephrine HCI 5mg

Terminated Labeling / mix-up LNK International, Inc. NDC 0363-6171-09 D-0014-2023

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

0363-0852 See recall 5
0363-0073 Soothe 2
0363-0441 See recall 2
0363-0620 Maximum Strength Hydrocortisone Cream with Aloe 2
0363-0638 Maximum Strength Hydrocortisone Cream 2
0363-0950 See recall 2

Yes — this exact package was recalled

Recalls naming this package

NDC 0363-6171-09 Walgreens Sinus Pressure

Other recalled products from this labeler

Know the day your medication is recalled