Hemorrhoid Pain Relief

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: Hemorrhoid Pain Relief
Generic name: LIDOCAINE
Manufacturer: Telebrands Corp
Product type: HUMAN OTC DRUG
SPL set ID: 04164425-ca3b-ef24-e063-6294a90a59d8
SPL ID: 275a333c-1c0c-e9f5-e063-6394a90ae3f5
Version: 3
Effective date: 2024-11-20
Source export date: 2026-09-28
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:15:40

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 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M015	openfda.application_number
brand name		Hemorrhoid Pain Relief	openfda.brand_name
generic name		LIDOCAINE	openfda.generic_name
manufacturer name		Telebrands Corp	openfda.manufacturer_name
ndc	package	73287-028-01	openfda.package_ndc
ndc	product	73287-028	openfda.product_ndc
ndc11	package	73287002801	derived:openfda.package_ndc
spl id		275a333c-1c0c-e9f5-e063-6394a90ae3f5	id
spl set id		04164425-ca3b-ef24-e063-6294a90a59d8	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 Allergy alert: If prone to allergic reaction from aspirin or salicylates, consult a doctor before use. When using this product do not exceed the recommended daily dosage unless directed by a doctor. use only as directed. Read and follow all directions and warnings on this label. do not put this product into the rectum by using finger or any mechanical device or applicator. Stop use and ask a doctor if if condition worsens or does not improve within 7 days in case of bleeding symptom being treated does not subside or if redness, irritation, swelling, pain, or other symptoms develop or increase. Certain persons can develop allergic reactions to ingredients in this product. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children and pets. 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.