Lidocaine anorectal cream

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: Lidocaine anorectal cream
Generic name: LIDOCAINE 5%
Manufacturer: EveryMarket Inc
Product type: HUMAN OTC DRUG
SPL set ID: 1604daec-812f-4684-ba98-fbcda07a7461
SPL ID: 51a1ad8e-1a05-61ab-e063-6394a90a7c4f
Version: 3
Effective date: 2026-05-12
Source export date: 2026-10-12
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/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:39:13

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		Lidocaine anorectal cream	openfda.brand_name
generic name		LIDOCAINE 5%	openfda.generic_name
manufacturer name		EveryMarket Inc	openfda.manufacturer_name
ndc	package	85833-001-04	openfda.package_ndc
ndc	product	85833-001	openfda.product_ndc
ndc11	package	85833000104	derived:openfda.package_ndc
rxcui		1366789	openfda.rxcui
spl id		51a1ad8e-1a05-61ab-e063-6394a90a7c4f	id
spl set id		1604daec-812f-4684-ba98-fbcda07a7461	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) • If condition worsens or does not improve within 7 days, consult a doctor. • Do not exceed the recommended daily dosage unless directed by a doctor. • In case of bleeding, consult a doctor promptly. • Do not put this product into the rectum by using fingers or any mechanical device or applicator. Stop and ask a doctor if -an allergic reaction occurs - symptom does not improve or if redness, irritation, swelling, pain or other symptom develop or increase.

Reported adverse events (FAERS/openFDA)#

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