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Posted April 15, 2017

Hyland's Baby Teething Tablets and Nighttime Teething Tablets Recalled

On April 13, 2017, Standard Homeopathic Company its Hyland's Baby Teething Tablets and Hyland's Baby Nighttime Teething Tablets because FDA testing has found the tablets contain inconsistent amounts of belladonna alkaloids that may differ from the calculated amount on the products' labels.

As noted in the press release, the FDA believes belladonna represents a serious health hazard to children and that the effects of belladonna are unpredictable.

The agency first announced the results of its testing in January 2017. Standard Homeopathic stopped making and shipping the medicines nationwide in October 2016 but did not issue a recall at that time.

Recalled Hyland's Baby Teething Tablets and Hyland's Baby Nighttime Teething Tablets include all lots and all products that retailers may have left in stock.

Consumers should contact their healthcare provider if they have experienced any adverse side effects. Consumers and healthcare providers are also encouraged to report any adverse reactions to the FDA's MedWatch Adverse Event Reporting Program.

See Related Warnings:

FDA Testing Confirms Elevated Levels of Belladonna in Some Homeopathic Teething Products

Homeopathic Teething Tablets and Ear Relief Products Containing Belladonna Recalled

Homeopathic Teething Tablets and Gels May Pose Danger, FDA Warns

Don't Rely on Homeopathic Asthma Products, FDA Warns

Weight Loss Supplement Recalled

Homeopathic Products Recalled Due to Allergy Risk

For more about the recall, use the link below.