Dr. Reddy's Laboratories, Inc. recalls Doan's Pain Relieving Cream with 4% Lidocaine Plus Menthol, (lidocaine 4%, menthol 1%), Net Wt. 2.75 oz. (77.3 g) Tube,
Labeling: Incorrect or Missing Lot and/or Exp Date; lot number on the secondary packaging doesnt match the lot number printed on the bottle
Recall notice
Labeling: Incorrect or Missing Lot and/or Exp Date; lot number on the secondary packaging doesnt match the lot number printed on the bottle
Contact the company & request your remedy
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Source Page by GovInfoNow · govinfonow.com/recall/41114-dr-reddy-s-laboratories-inc-recalls-doan-s-pain-relieving · Recall date October 30, 2017 · FDA enforcement record: FDA #D-0072-2018
Cite this page
“Dr. Reddy's Laboratories, Inc. recalls Doan's Pain Relieving Cream with 4% Lidocaine Plus Menthol, (lidocaine 4%, menthol 1%), Net Wt. 2.75 oz. (77.3 g) Tube,.” GovInfoNow, recall dated October 30, 2017. https://govinfonow.com/recall/41114-dr-reddy-s-laboratories-inc-recalls-doan-s-pain-relieving. Based on FDA recall #D-0072-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0072-2018%22&limit=1).
How to tell if you have this one
- Brand
Dr. Reddy's Laboratories, Inc.- Product
Doan's Pain Relieving Cream with 4% Lidocaine Plus Menthol, (lidocaine 4%, menthol 1%), Net Wt. 2.75 oz. (77.3 g) Tube- Category
Drug
Contact Dr. Reddy's Laboratories, Inc.
We’ve drafted a message you can send Dr. Reddy's Laboratories, Inc. to request your refund or repair — edit it as you like.
Subject: Recall D-0072-2018 — Dr. Reddy's Laboratories, Inc. Doan's Pain Relieving Cream with 4% Lidocaine Plus Menthol, (lidocai Hello, I own a Doan's Pain Relieving Cream with 4% Lidocaine Plus Menthol, (lidocaine 4%, menthol 1%), Net Wt. 2.75 oz. (77.3 g) Tube that is covered by recall D-0072-2018 from Dr. Reddy's Laboratories, Inc.. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0072-2018 (October 30, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0072-2018 to see it in context.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.