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

Is NDC 0536-1271-80 recalled?

First Aid Antiseptic · 1 TUBE in 1 BOX (0536-1271-80) / 28.4 g in 1 TUBE

Yes — this exact package was recalled

1 FDA recall names the code 0536-1271-80 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
Povidone-Iodine
Strength
POVIDONE-IODINE 100 mg/g
Form
Ointment · Topical
Labeler
Rugby Laboratories
Type
Human OTC Drug
Product code
0536-1271

Recalls naming this package

Class II · Moderate risk

First Aid Antiseptic Ointment

Incorrect/Undeclared Excipients: The inactive ingredients labeled on the product boxes and tubes are listed as "mineral oil , petrolatum ". The inactive ingredients in the actual product are polyethylene glycol 400 , polyethylene glycol 4000.

Ongoing Chemical / undeclared Zhejiang Jingwei Pharmaceutical Co., Ltd. D-0013-2025

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