When using this product frequent or prolonged use may result in dependence on laxatives, may take up to 3 days for you to have a bowel movement. Stop use and ask a doctor if rectal bleeding occurs, symptoms persist, last for more than 7 days. Ask a doctor or pharmacist before use if you noticed a sudden change in bowel habits that has lasted longer than 2 weeks (this may be a sign of a serious condition), are pregnant or breastfeeding. 6, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, purified water, silicon dioxide, sodium benzoate, stearic acid, titanium dioxide.Ĭaution: Do not use if you have abdominal pain, nausea, fever, vomiting, with other medicines or if you are presently taking mineral oil, if you are on a low salt diet, longer than 7 days. Inactive ingredients: Carnauba wax, croscarmellose sodium, D&C Yellow No. Do not take more than 8 tablets in 24 hours, drink lots of fluids (one full glass or more). Recommended Dosage: (Adults and children 12 years and older) Take 2 to 4 tablets at bedtime or twice daily with a glass of water. Healthcare professionals and consumers should report any adverse reactions or quality problems they experienced using the product to MedWatch, FDA’s Safety Information and Adverse Event Reporting Program.Rexall Senna Laxative and Docusate Sodium Tablets. Consumers should contact their healthcare provider if they experience any health problems potentially related to the product. Patients and consumers with questions regarding the recall can contact Vi-Jon, LLC, at from 7:30 am–4:30 pm CST. Consumers and healthcare providers should stop using any of the affected lots and return any remaining product. Vi-Jon, LLC, is investigating three reports of serious adverse reactions potentially related to the recall.įDA reported that Vi-Jon, LLC, notified customers by phone and email and is arranging for return of all recalled product. The product was distributed to wholesale and retail outlets nationwide. The following products are now included:Įquate 10 oz grape magnesium citrate syrup On July 26, 2022, FDA reported that Vi-Jon, LLC, expanded the recall to include all lots of all flavors the product at the consumer level. NDC-national drug code UPC-universal product code Signature Care 10 oz lemon magnesium citrate Quality Choice 10 oz lemon magnesium citrate Premier Value 10 oz low sodium lemon citrate Health Mart 10 oz lemon magnesium citrate Harris Teeter 10 oz lemon magnesium citrate The following products are now included:īest Choice 10 oz lemon magnesium citrateĭiscount Drug Mart 10 oz lemon magnesium citrateĮquate 10 oz lemon magnesium citrate syrupĮxchange Select 10 oz lemon magnesium citrate On July 14, 2022, FDA reported that Vi-Jon, LLC, expanded the recall to include all lots of the product at the consumer level. The recalled lot was distributed to CVS drug stores nationwide. The affected lot’s batch number is 0556808 and has the expiration date of 12/2023, both of which are printed on the bottle’s shoulder. To date, Vi-Jon, LLC, has not reported any complaints related to the recall. In the recall, Vi-Jon, LLC, advised that immunocompromised patients who consume this product may be at increased risk for infections that could lead to life-threatening adverse health consequences.
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