Flarestop Hemorrhoid Lidocaine

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: Flarestop Hemorrhoid Lidocaine
Generic name: LIDOCAINE
Manufacturer: Chelsea Pharmacceuticals LLC
Product type: HUMAN OTC DRUG
SPL set ID: b8a589f7-7131-4807-9bcb-84af3078e258
SPL ID: 5b08135d-6813-2a1e-e063-6394a90abc28
Version: 1
Effective date: 2026-09-10
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:27:02

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M015	openfda.application_number
brand name		Flarestop Hemorrhoid Lidocaine	openfda.brand_name
generic name		LIDOCAINE	openfda.generic_name
manufacturer name		Chelsea Pharmacceuticals LLC	openfda.manufacturer_name
ndc	package	87989-013-00	openfda.package_ndc
ndc	product	87989-013	openfda.product_ndc
ndc11	package	87989001300	derived:openfda.package_ndc
rxcui		1366789	openfda.rxcui
spl id		5b08135d-6813-2a1e-e063-6394a90abc28	id
spl set id		b8a589f7-7131-4807-9bcb-84af3078e258	set_id
unii		98PI200987	openfda.unii

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 For external use only Do Not Exceed the recommended daily dosage unless directed by a doctor. put this product into the rectum by using your fingers or any mechanical device or applicator. When using this product If the condition worsens or does not improve within 7 days, consult a doctor. In case of bleeding, consult a doctor promptly. Stop use and ask a doctor if If the symptoms being treated do not subside or if redness, irritation, swelling, pain, or other symptoms develop or increase. Allergy alert Certain persons can develop allergic reactions to ingredients in this product. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. If pregnant or breast-feeding, ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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