Morning After Pill

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
Morning After Pill
Generic name
LEVONORGESTREL
Manufacturer
Cadence Health Inc
Product type
HUMAN OTC DRUG
SPL set ID
2fb59f53-d885-9d4a-e063-6394a90a88cc
SPL ID
32e9d9ba-b359-4826-e063-6294a90a927b
Version
2
Effective date
2025-04-15
Source export date
2026-10-12
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:11:08
Harmonized routes table
Harmonized routes
ORAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Allergy Alert: Do not use if you have ever had an allergic reaction to levonorgestrel Sexually transmitted diseases (STDs) Alert: This product does not protect against HIV/AIDS or other STDs

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.