Bloop Fissure Healing Anorectal Topical

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: Bloop Fissure Healing Anorectal Topical
Generic name: LIDOCAINE
Manufacturer: Three Nations Corp
Product type: HUMAN OTC DRUG
SPL set ID: 0b645092-ebc4-e4bb-e063-6294a90ad4cf
SPL ID: 0b645092-ebc3-e4bb-e063-6294a90ad4cf
Version: 1
Effective date: 2023-11-30
Source export date: 2026-10-27
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/977776a6cc37ec1c77259da8a93ae161850a3aa120341096e5a03428b84d016b/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:56:34

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		Bloop Fissure Healing Anorectal Topical	openfda.brand_name
generic name		LIDOCAINE	openfda.generic_name
manufacturer name		Three Nations Corp	openfda.manufacturer_name
ndc	package	83838-153-01	openfda.package_ndc
ndc	product	83838-153	openfda.product_ndc
ndc11	package	83838015301	derived:openfda.package_ndc
rxcui		1366789	openfda.rxcui
spl id		0b645092-ebc3-e4bb-e063-6294a90ad4cf	id
spl set id		0b645092-ebc4-e4bb-e063-6294a90ad4cf	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

For external use only (skin of the perianal area and anal canal). When using this product do not exceed recommended 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 condition worsens or does not improve within 7 days rectal bleeding occurs 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

Reported adverse events (FAERS/openFDA)#

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