PlainRecalls
FDA Drug Low Class III Terminated

Select Brand Cough Control CF Max, Maximum Strength for MUCUS RELIEF, (dextromethorphan HBr 10 mg, guaifenesin 200 mg, phenylephrine HCI 5 mg), 4 fl.oz 12pk (NDC 15127-025-04; UPC Code: 0-15127-02535-5), Distributed by: Select Brand Distributors, Pine Bluff, AR 71603 USA.

Reported: March 13, 2013 Initiated: January 18, 2013 #D-187-2013

Product Description

Select Brand Cough Control CF Max, Maximum Strength for MUCUS RELIEF, (dextromethorphan HBr 10 mg, guaifenesin 200 mg, phenylephrine HCI 5 mg), 4 fl.oz 12pk (NDC 15127-025-04; UPC Code: 0-15127-02535-5), Distributed by: Select Brand Distributors, Pine Bluff, AR 71603 USA.

Reason for Recall

Presence of Precipitate; white substance confirmed as Guaifenesin, an active ingredient was observed in some bottles. If the product is shaken or warmed the white particles goes into the solution.

Details

Recalling Firm
Aaron Industries Inc
Units Affected
5,676 bottles (473 cases)
Distribution
Nationwide
Location
Lynwood, CA

Frequently Asked Questions

What product was recalled? ▼
Select Brand Cough Control CF Max, Maximum Strength for MUCUS RELIEF, (dextromethorphan HBr 10 mg, guaifenesin 200 mg, phenylephrine HCI 5 mg), 4 fl.oz 12pk (NDC 15127-025-04; UPC Code: 0-15127-02535-5), Distributed by: Select Brand Distributors, Pine Bluff, AR 71603 USA.. Recalled by Aaron Industries Inc. Units affected: 5,676 bottles (473 cases).
Why was this product recalled? ▼
Presence of Precipitate; white substance confirmed as Guaifenesin, an active ingredient was observed in some bottles. If the product is shaken or warmed the white particles goes into the solution.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on March 13, 2013. Severity: Low. Recall number: D-187-2013.

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