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The consumer healthcare company is recalling the cough syrup, sold under the brand name "Robitussin Honey CF Max Day Adult" in 4-ounce and 8-ounce doses, along with its 8-ounce night-time version.
The maker of Robitussin cough syrup is recalling several lots of products containing honey due to contamination that could pose a serious risk to people with weakened immune systems. Haleon’s ...
Haleon is recalling eight lots of Robitussin cough syrup sold nationwide due to a microbial contamination. Consumers with questions can contact Haleon by phone at 1-800-245-1040 or by email at ...
Medication could contain dangerously high levels of yeast WASHINGTON (AP) — The maker of Robitussin cough syrup is recalling several […] The post Robitussin maker recalls several lots of cough ...
Due to dextromethorphan's selective serotonin reuptake inhibitor-like action, the sudden cessation of recreational dosing in tolerant individuals can result in mental and physical withdrawal symptoms similar to the withdrawal from SSRIs. These withdrawal effects can manifest as psychological effects, including depression, irritability, cravings ...
FDA's role under the guidelines is to monitor company recalls and assess the adequacy of a firm's action. After a recall is completed, FDA makes sure that the product is destroyed or suitably reconditioned and investigates why the product was defective. Generally, FDA accepts reports and other necessary recall information submitted by e-mail.
A drug recall removes a prescription or over-the-counter drug from the market. Drug recalls in the United States are made by the FDA or the creators of the drug when certain criteria are met. When a drug recall is made, the drug is removed from the market and potential legal action can be taken depending on the severity of the drug recall. [1]
If you have any questions regarding the product or the recall, they can be directed to Haleon’s consumer relations team at +1-800-245-1040 (Monday through Friday 8:00 a.m. to 6:00 p.m. EST) or ...