Class II ยท Moderate risk
PVP Scrub Solution
Subpotent Drug: product not meeting the iodine assay level requirements through the labeled expiry.
National Drug Code
Is NDC 53329-0938-04 recalled?
Povidone-Iodine · 118 mL in 1 BOTTLE (53329-938-04)
Yes — this exact package was recalled
1 FDA recall names the code 53329-0938-04 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
- Povidone-Iodine
- Strength
- POVIDONE-IODINE .75 g/100mL
- Form
- Solution · Topical
- Labeler
- Medline Industries, LP
- Type
- Human OTC Drug
- Product code
- 53329-0938
Recalls naming this package
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
- 53329-0303 See recall 2
- 53329-0811 Medline Alcohol Prep Sterile, Large 2
- 53329-0827 Curad Alcohol Prep Pads Medium 2
- 53329-0066 See recall 1
- 53329-0081 See recall 1
- 53329-0083 SparkleFresh Flouride Toothpaste 1
Free recall alerts
Know the day your medication is recalled
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