NumbMD Lidocaine Cream Anorectal(hemorrhoidal)

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: NumbMD Lidocaine Cream Anorectal(hemorrhoidal)
Generic name: LIDOCAINE 5%
Manufacturer: EveryMarket Inc
Product type: HUMAN OTC DRUG
SPL set ID: 52379055-d017-4d98-e063-6294a90a196c
SPL ID: 58da7d16-d941-920a-e063-6294a90aae31
Version: 2
Effective date: 2026-08-12
Source export date: 2026-11-06
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/97001096994db9ca8cee114e6c3bb5298d3c573158ffc1ab8692d82e76a3eb40/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 06:56:11

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		NumbMD Lidocaine Cream Anorectal(hemorrhoidal)	openfda.brand_name
generic name		LIDOCAINE 5%	openfda.generic_name
manufacturer name		EveryMarket Inc	openfda.manufacturer_name
ndc	package	85833-006-01	openfda.package_ndc
ndc	product	85833-006	openfda.product_ndc
ndc11	package	85833000601	derived:openfda.package_ndc
rxcui		1366789	openfda.rxcui
spl id		58da7d16-d941-920a-e063-6294a90aae31	id
spl set id		52379055-d017-4d98-e063-6294a90a196c	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 If condition worsens or does not improve within 7 days, consult a doctor. Do not exceed the recommended dailydosage, unless directed by a doctor. in case of bleeding, consult a doctor promptly. Do not put this product into the rectum byusing fingers or any mechanical device or applicator. an llergic reaction occurs. symptom does not improve or if redness, irritation, swelling, pain or other symptom developor increase. ask a health professional before use. In case of accidental ingestion, seek medical advice immediately or contact a Poison Control Center right away. (1-800-222-1222)

Reported adverse events (FAERS/openFDA)#

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