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Class III: unlikely to cause harmTerminated

Poly-Tussin Ac Liquid Recall

POLY-TUSSIN AC LIQUID, Each 5 mL (1 teaspoonful) contains: Brompheniramine Maleate 4 mg…

Poly Pharmaceuticals, Inc · Owens Cross Roads, AL

Risk level
Class III
Reported by FDA
Jul 23, 2014
Recall ID
D-1431-2014
Check your lot numberHow we source this data

Summary

Poly Pharmaceuticals recalled Poly-Tussin Ac Liquid starting Jun 26, 2014. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report D-1431-2014 on Jul 23, 2014. Reason: Does Not Meet Monograph: Phenylephrine and pseudoephedrine are below monograph specifications, and label inaccurately contains wording "Rx Only". Status: Terminated.

Why it was recalled

Does Not Meet Monograph: Phenylephrine and pseudoephedrine are below monograph specifications, and label inaccurately contains wording "Rx Only".

Product description

POLY-TUSSIN AC LIQUID, Each 5 mL (1 teaspoonful) contains: Brompheniramine Maleate 4 mg, Codeine Phosphate 10 mg, Phenylephrine HCl 7.5 mg, 16 fl oz. (473 mL) Bottle, Rx Only. Manufactured by: Great Southern Laboratories, Houston, TX 77099, Distributed for: Poly Pharmaceuticals, Mobile, AL 36619. NDC: 50991-713-16.

Lot numbers, UPCs & expiration codes

Lot #: 04413, Expiry: 02/15

Where it was sold

U.S. Nationwide

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-1431-2014
Classification
Class III
Status
Terminated
Recall initiated
Jun 26, 2014
FDA report date
Jul 23, 2014
Quantity
208 Bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Poly Pharmaceuticals, Inc

Original FDA data

Every field from FDA enforcement report D-1431-2014, exactly as published.

Show all FDA fields
City
Owens Cross Roads
State
AL
Status
Terminated
Country
United States
Event ID
68671
Address
2720 Cullom Blvd Se
Code information
Lot #: 04413, Expiry: 02/15
Postal code
35763-9309
Report date
Jul 23, 2014
Product type
Drugs
Recall number
D-1431-2014
Classification
Class III
Recalling firm
Poly Pharmaceuticals, Inc
Product quantity
208 Bottles
Termination date
Nov 3, 2014
Reason for recall
Does Not Meet Monograph: Phenylephrine and pseudoephedrine are below monograph specifications, and label inaccurately contains wording "Rx Only".
Voluntary / mandated
Voluntary: Firm initiated
Product description
POLY-TUSSIN AC LIQUID, Each 5 mL (1 teaspoonful) contains: Brompheniramine Maleate 4 mg, Codeine Phosphate 10 mg, Phenylephrine HCl 7.5 mg, 16 fl oz. (473 mL) Bottle, Rx Only. Manufactured by: Great Southern Laboratories, Houston, TX 77099, Distributed for: Poly Pharmaceuticals, Mobile, AL 36619. NDC: 50991-713-16.
Distribution pattern
U.S. Nationwide
Recall initiation date
Jun 26, 2014
Initial firm notification
Letter
Center classification date
Jul 11, 2014

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1431-2014, published Jul 23, 2014. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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