FDA.reportPublic FDA data

Femarone 20

openFDA label record#

Cross-check layer: This is openFDA JSON-derived label data. Use the corresponding DailyMed SPL as the canonical label.

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

Brand name
Femarone 20
Generic name
FEMARONE 20
Manufacturer
Wise Essentials LLC
Product type
HUMAN OTC DRUG
SPL set ID
44ea74ce-2ba1-e578-e063-6394a90ab72d
SPL ID
44ea74ce-2ba2-e578-e063-6394a90ab72d
Version
1
Effective date
2025-12-13
Source export date
2026-08-01
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/286b06ef66f7efdb8cdf48688678b429950d1b94558fe44fcd6cc6eb20c2100b/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:04:58
Harmonized routes table
Harmonized routes
TRANSDERMAL

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: If pregnant or nursing or if you have a serious medical condition, consult a healthcare professional before using this product. KEEP OUT OF REACH OF CHILDREN Store in a cool, dry place Always consult your healthcare provider before using or if pregnant or nursing. Cease use and seek medical attention if skin irritation or a negative reaction. Keep out of reach of children. Store in a cool, dry place. California Prop 65 Law requires this statement: This product contains progesterone, a chemical known only to the State of California to cause cancer. Cease using this product and seek medical attention if skin irritation or other negative reactions occur.