Class II ยท Moderate risk
TRIFLUENT PHARMA TRIDERGEL Wound Care Gel
CGMP Deviations: product manufactured in the same facility under the same conditions as the product found to be contaminated
National Drug Code
Is NDC 73352-0520-01 recalled?
Tridergel · 29.6 mL in 1 BOTTLE, WITH APPLICATOR (73352-520-01)
Yes — this exact package was recalled
1 FDA recall names the code 73352-0520-01 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
- Benzalkonium Chloride
- Strength
- BENZALKONIUM CHLORIDE .001 g/mL
- Form
- Gel · Topical
- Labeler
- Trifluent Pharma LLC
- Type
- Human OTC Drug
- Product code
- 73352-0520
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
- 73352-0550 Tripenicol S 1
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.