The Femme Fix Hemorrhoid Treatment

openFDA label record#

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

Brand name
The Femme Fix Hemorrhoid Treatment
Generic name
LIDOCAINE, PHENYLEPHRINE HYDROCHLORIDE
Manufacturer
POPPY COLLECTIVE LLC
Product type
HUMAN OTC DRUG
SPL set ID
5217b5d9-b835-4428-a6b3-e6b255630742
SPL ID
35b65b6c-4694-b4f1-e063-6394a90a4325
Version
1
Effective date
2025-05-27
Source export date
2026-09-28
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:14:32
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only. Allergy Alert Certain persons can develop allergic reactions to ingreadients in this product Ask a doctor before use if you have: –Heart disease; high blood pressure; thyroid disease; diabetes. –Difficulty in urination due to enlargement of the prostate gland. Ask a doctor or pharmacist before use if you are presently taking a prescription drug for high blood pressure or depression. When using this product –Avoid contact with eyes. –Do not exceed recommended daily dosage unless directed by a doctor. –Do not put this product into the rectum by using fingers or any mechanical device or applicator. Stop use and ask a doctor if –Bleeding occurs. –Condition worsens or does not improve within 7 days. –Allergic reaction occurs to ingredients in this product. –Symptom being treated does not subside or if redness, irritation, swelling, pain or other symptoms develop or increase. If pregnant or breast-feeding, ask a doctor before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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