On Friday, Maharashtra’s Food and Drugs Administration said that it had revoked the product production licence for Johnson’s Baby Powder, which is made by Johnson’s & Johnson’s Private Limited.
The Maharashtra FDA released a press release indicating that the Johnson’s Baby Powder samples were deemed “Not of Standard Quality.” Johnson’s Baby Powder samples were collected by FDA Maharashtra in Pune and Nashik for quality control.
“The sample does not comply with IS 5339: 2004 (Second Revision Amendment No. 3) Specification for Skin powder for infants in the test pH,” the press note stated.
The administration issued show cause notice to the firm under the Drugs and Cosmetics Act, 1940 and also issued instructions to the firm to recall the stock of the said product from the market.
As per the press note, the firm also challenged the quality tests to be sent to the Central Drugs Laboratory (CDL) Government of India. However, the Director of CDL also issued the final conclusive report in line with the Maharashtra FDA.
“Since Johnson’s Baby Powder is used in newborn babies, the sample being declared “Not of Standard in pH” may affect the health of the skin of the newborn babies. Hence, in the larger public interest, FDA Maharashtra is cancelling the manufacturing licence of the Johnson’s Baby Powder, with the order dated September 15,” the press note further said.
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