Nupharmisto NumbMD 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 Lidocaine Cream
Generic name: LIDOCAINE 5%
Manufacturer: EveryMarket Inc
Product type: HUMAN OTC DRUG
SPL set ID: 52369a41-820d-cd7a-e063-6394a90ac6d1
SPL ID: 58da9238-cce3-62f9-e063-6394a90af2be
Version: 2
Effective date: 2026-08-12
Source export date: 2026-11-06
Source partition: 14
Source file: https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/2cac198adf50bf0f7077ca012f418bbee1fb171f907f83d6a83048d9770d345b/drug-label-0014-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 08:11:57

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 Lidocaine Cream	openfda.brand_name
generic name		LIDOCAINE 5%	openfda.generic_name
manufacturer name		EveryMarket Inc	openfda.manufacturer_name
ndc	package	85833-005-01	openfda.package_ndc
ndc	product	85833-005	openfda.product_ndc
ndc11	package	85833000501	derived:openfda.package_ndc
rxcui		1366789	openfda.rxcui
spl id		58da9238-cce3-62f9-e063-6394a90af2be	id
spl set id		52369a41-820d-cd7a-e063-6394a90ac6d1	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 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.

Reported adverse events (FAERS/openFDA)#

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