Class II โ€” Potential Health Hazard

Potential health hazard โ€” use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Eye Drops advanced relief (Dextran 70 0.1% Recalled by K C Pharmaceuticals Inc Due to Labeling: Label Mix-Up: Incorrect back labeling of the...

Date: March 1, 2010
Company: K C Pharmaceuticals Inc
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact K C Pharmaceuticals Inc directly.

Affected Products

Eye Drops advanced relief (Dextran 70 0.1%, Polyethylene glycol 400 1%, Povidone 1%, Tetrahydrozoline HCl 0.05%) ophthalmic solution, 1/2 fl oz (15 mL) bottle, Distributed By Dolgencorp, LLC, 100 Mission Ridge, Goodlettsville, TN 37072.

Quantity: 31,704 bottles

Why Was This Recalled?

Labeling: Label Mix-Up: Incorrect back labeling of the immediate container of eye drops (unit carton and front label are correct) which do not list three active ingredients: Dextran 70, PEG 400, and povidone.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About K C Pharmaceuticals Inc

K C Pharmaceuticals Inc has 5 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report