Nupharmisto NumbMD 5% Lidocaine 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: Nupharmisto NumbMD 5% Lidocaine cream
Generic name: LIDOCAINE 5%
Manufacturer: EveryMarket Inc
Product type: HUMAN OTC DRUG
SPL set ID: 507d0c2c-9517-40f8-e063-6394a90a1996
SPL ID: 58da9b79-ea96-ae8c-e063-6294a90a93df
Version: 2
Effective date: 2026-08-12
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:56:15

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		Nupharmisto NumbMD 5% Lidocaine cream	openfda.brand_name
generic name		LIDOCAINE 5%	openfda.generic_name
manufacturer name		EveryMarket Inc	openfda.manufacturer_name
ndc	package	85833-003-01	openfda.package_ndc
ndc	product	85833-003	openfda.product_ndc
ndc11	package	85833000301	derived:openfda.package_ndc
rxcui		1366789	openfda.rxcui
spl id		58da9b79-ea96-ae8c-e063-6294a90a93df	id
spl set id		507d0c2c-9517-40f8-e063-6394a90a1996	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 imiprove 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 a pplicator. 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. If pregnant or breast-feeding , ask a health professional before use. In case of accidental ingestion, seek medecal 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.