Class II · Moderate risk
DuraPrep Surgical Solution Iodine Povacrylex
Chemical contamination: Product may be contaminated with a toxic compound.
National Drug Code
Is NDC 17518-0011-07 recalled?
3M DuraPrep Surgical · 1 APPLICATOR in 1 CASE (17518-011-07) / 6 mL in 1 APPLICATOR
Yes — this exact package was recalled
1 FDA recall names the code 17518-0011-07 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
- Iodine Povacrylex and Isopropyl Alcohol
- Strength
- IODINE POVACRYLEX 6.02 mg/mL; ISOPROPYL ALCOHOL 636.4 mg/mL
- Form
- Solution · Topical
- Labeler
- Solventum US LLC
- Type
- Human OTC Drug
- Product code
- 17518-0011
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.
Free recall alerts
Know the day your medication is recalled
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