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If you ve got this popular skin cream, stop using it immediately

If You re Using This Cream, Stop Immediately

If You re Using This Cream, Stop Immediately By John Quinn of Best Life | If You re Using This Cream, Stop Immediately A recall has been issued on a popular anesthetic cream this week, with authorities warning consumers to check if they have recently purchased one brand in particular. The recall alert was reported by the United States Consumer Product Safety Commission (CPSC) and is due to the product s packaging not being child-safe. Read on to see if you have this cream at home, and for another product to be on the lookout for, check out If You Have These Microwave Meals at Home, Get Rid of Them Now.

Scalpa Numb Maximum Strength Topical Anesthetic Cream Being Recalled

Scalpa Numb Maximum Strength Topical Anesthetic Cream Being Recalled WASHINGTON (dpa-AFX) - Phoenix, Arizona-based Scalpa Inc. has recalled Scalpa Numb Maximum Strength Topical Anesthetic Cream citing risk of poisoning as it failed to meet child resistant packaging requirements, according to the U.S. Consumer Product Safety Commission. The recall involves about 10,000 units of the Anesthestic Cream in a 10 gram black and white tube with a white cap. SCALPANUMB and Maximum Strength Topical Anesthetic Cream are printed on the label. The affected product s expiration date is marked as EXP 202307 on the crimped end of the tube. Batch number 1000000101, Code: C1 and the UPC code 857076008689 are printed on the outside of the box.

Wintergreen Oil Market 2021 Global Trends, Share, Growth, Analysis, Opportunities and Forecast To 2025

Excedrin recalls 400k bottles of headache medicine for packaging issues, risk of poisoning

Excedrin recalls 400k bottles of headache medicine for packaging issues, risk of poisoning Published: January 5, 2021 6:51 PM EST Recommended Around 433,600 bottles of Excedrin products are being recalled because some of the bottles may have a hole in the bottom. The plastic bottles pose a poisoning risk, if there’s a hole, because a child may be able to get the caplets and swallow the painkillers. GSK Consumer Health issued the recall for five types of Excedrin products toward the end of December 2020. Consumers should immediately check Excedrin bottles to see if there is a hole at the bottom. If there isn’t a hole, the consumers can keep the over-the-counter medicine, according to the recall.

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