Health & Fitness

Children’s Advil Recall, Potential Overdose: How To Check Labels

Some 28,000 bottles of bubble-gum flavored Children's Advil was recalled because dosage cap markings could cause some to overdose.

Check your medicine cabinets, parents. Pfizer has recalled 28,000 bottles of its bubble-gum flavored Children’s Advil pain reliever because incorrect markings on the dosage cup may cause some children to overdose. The cup markings are in teaspoons and the instructions on the label are in milliliters, the company said.

A teaspoon contains approximately five milliliters. Pfizer Consumer Healthcare, a division of Pfizer Inc., said one lot of the 4-ounce bottles of bubble-gum flavored Children’s Advil Suspension were distributed nationwide in May and June.

To see the bottle you bought is included in the recall, they have a November 2020 expiration date, the marked code R51129 and a UPC number 3-0573-0207-30-0.

Find out what's happening in Across Americafor free with the latest updates from Patch.


(Get Across America Patch’s daily newsletter and real-time news alerts. Or, find your local Patch here and subscribe. Like us on Facebook. Also, download the free Patch iPhone app or free Patch Android app.)


Children’s Advil is commonly used for fevers and minor pain relief from conditions like colds, flu, sore throat, headaches and toothaches.The most common symptoms associated with ibuprofen overdose include nausea, vomiting, headache, drowsiness, blurred vision and dizziness.

Find out what's happening in Across Americafor free with the latest updates from Patch.

Pfizer said it notified wholesalers, distributors and retailers to arrange for the return of any recalled products, stop distributing it immediately and contact any outlets that might be selling it. About one third of the bottles never made it to market, a Pfizer spokesperson told CBS News.

What you should do if you have an affected bottle:

  • For instructions on returning product or additional assistance, call Stericycle at (800) 805- 3093 from 8 a.m.-5 p.m. EDT, Monday through Friday.
  • For questions regarding the recall or to report an adverse event, call the Pfizer Consumer Healthcare information line at (800) 882-3845, from 9 a.m.-5 p.m. EDT, Monday through Friday.

For more on this recall, go here.

Photo via Pfizer Inc.

Get more local news delivered straight to your inbox. Sign up for free Patch newsletters and alerts.