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: 51d370b4-1c34-d203-e063-6394a90a80b1
SPL ID: 58da9593-5e66-6430-e063-6394a90ac8b2
Version: 2
Effective date: 2026-08-12
Source export date: 2026-09-28
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/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:26:46

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	85833-004-01	openfda.package_ndc
ndc	product	85833-004	openfda.product_ndc
ndc11	package	85833000401	derived:openfda.package_ndc
rxcui		1366789	openfda.rxcui
spl id		58da9593-5e66-6430-e063-6394a90ac8b2	id
spl set id		51d370b4-1c34-d203-e063-6394a90a80b1	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 conditin 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 by using fingers or any mechanical device or applicator. an allergic reaction occurs. symptom does not improve or if redness, irritation, swelling, pain or other symptom develop or 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.