# FDA recall D-192-2013

> **K C Pharmaceuticals Inc** · Class II · drug recall initiated 2010-03-01.

## Product

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.

## Reason for recall

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.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-192-2013
- **Recalling firm:** K C Pharmaceuticals Inc
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2010-03-01
- **Report date:** 2013-03-20
- **Termination date:** 2013-04-02

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Pomona, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-192-2013

## Citation

> AI Analytics. FDA recall D-192-2013. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-192-2013. Source: US FDA. Licensed CC0.

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