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UAE recalls batch of Babies' Magic Tea gripe water over undeclared alcohol

The Emirates Drug Establishment ordered a recall of a batch of Babies' Magic Tea Baby Sleep Gripe Water after undeclared alcohol was found and the product was found to lack UAE marketing approval.

2 outlets · 0L · 2C · 0R First reported Account updated
Image: Gulf News
Image: The National

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The story, neutrally told

Centre · 1The Emirates Drug Establishment (EDE) has ordered the recall of an affected batch of Babies' Magic Tea – Baby Sleep Gripe Water after detecting undeclared alcohol in the product. Centre · 2The recall was announced under Administrative Circular No. 45 of 2026, and the authorities also cited the product's lack of valid marketing authorisation in the UAE. Centre · 1The National reports that the Dubai Health Authority (DHA) was also involved, and that a DHA circular urged healthcare facilities and medical practitioners to comply with the EDE's instructions.

Centre · 1Gulf News reports that health regulatory and supervisory authorities circulated the notice to pharmaceutical establishments, instructing them to carry out the withdrawal. Centre · 1The product, also called Children's Sleep Gripe Water, is marketed as a dietary supplement to relieve colic and gas and promote sleep in babies, and its packaging also claims to relieve constipation, acid reflux and fussiness. Centre · 1Consumers, parents and caregivers are told to stop using the product and either discard it or return it to the place of purchase for a refund; the batch number and expiry date were not specified.

Centre · 1The National adds that, according to the US Food and Drug Administration, Pacific Health Sciences voluntarily recalled one lot of the 4oz bottles earlier this month; FDA testing of lot 25122bw found undeclared ethanol, methanol and isopropanol at about 8.3, 0.35 and 0.48 per cent respectively. Centre · 1The FDA said the substances may pose a risk depending on the amount consumed and the person's age and body weight; infant ethanol exposure has been linked to long-term developmental consequences, and amounts recommended on the packaging can cause drowsiness, incoordination, nausea and vomiting, while higher amounts raise the risk of respiratory depression.

Every sentence links to the reporting it rests on. The pill in front of each says where its sources sit: Left, Centre or Right when one side supplies at least half of them, Mixed when they are evenly split. The number is how many outlets it cites.

Left0 outlets

No left outlet in our sources has covered this story yet.

Centre2 outlets

Framing
Both outlets report the recall as a straightforward regulatory notice. Gulf News is brief and focuses on the EDE order and compliance instructions. The National adds consumer advice and the US FDA test findings.
Emphasis
Gulf News stresses regulatory procedure; The National stresses health risks and the FDA findings.
Leaves out or plays down
Gulf News gives no consumer advice or test results. Neither specifies the batch number or expiry date.
For example
“The EDE urged healthcare facilities and medical professionals to comply with the circular” — Gulf News
“The batch number and expiry date were not specified.” — The National

Right0 outlets

No right outlet in our sources has covered this story yet.

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