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FDA Changes Plan B Label, Clarifies It Won’t Cause Abortion


WASHINGTON (AP) — The Food and Drug Administration announced Friday that it will overhaul packaging labels for the emergency contraceptive pill, Plan B, that women can take after having sex to prevent a pregnancy.

The federal agency said it will remove references on the contraception’s packaging that claim, without scientific evidence, that the pill prevents a fertilized egg from implanting in the womb.

The new labels are intended to further distinguish the emergency contraception — also known as the morning after pill — from abortion pills, which end a pregnancy after a fertilized egg has implanted in the lining of a woman’s uterus.

In a memo released Friday, the FDA clarified that taking Plan B pills is not the same as an abortion, a fact that has long been understood in the medical community.

“Evidence does not support that the drug affects implantation or maintenance of a pregnancy after implantation, therefore it does not terminate a pregnancy,” the FDA said in its statement.

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The agency added that the emergency contraception works similarly to birth control in preventing pregnancy, but contains a higher dose of levonorgestrel. The pill prevents ovulation.

The Food and Drug Administration has approved Plan B for use up to 72 hours, or three days, after unprotected sex. Women are able to get the emergency contraception over the counter.

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