Numb520

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: Numb520
Generic name: LIDOCAINE
Manufacturer: Clinical Resolution Laboratory, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: a0411950-c6ee-4427-acb6-3cef58b0e93e
SPL ID: 3532117c-c64a-14b2-e063-6394a90a7016
Version: 3
Effective date: 2025-05-15
Source export date: 2026-09-28
Source partition: 5
Source file: https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:33:49

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 · 13 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M015	openfda.application_number
brand name		Numb520	openfda.brand_name
generic name		LIDOCAINE	openfda.generic_name
manufacturer name		Clinical Resolution Laboratory, Inc.	openfda.manufacturer_name
ndc	package	63742-033-02	openfda.package_ndc
ndc	package	63742-033-01	openfda.package_ndc
ndc	product	63742-033	openfda.product_ndc
ndc11	package	63742003301	derived:openfda.package_ndc
ndc11	package	63742003302	derived:openfda.package_ndc
rxcui		1366789	openfda.rxcui
spl id		3532117c-c64a-14b2-e063-6394a90a7016	id
spl set id		a0411950-c6ee-4427-acb6-3cef58b0e93e	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) Do not use this product if pregnant or breastfeeding, ask a health professional before use. in case of accidental overdose, get medical help or contact the Poison Control Center immediately. seal is broken or missing. When using this product do not exceed the recommended daily dosage unless directed by a doctor. certain persons can develop allergic reactions to ingredients in this product. do not put this product into the rectum by using finger or any medical device or applicator. Stop use and ask a doctor if the symptom being treated does not subside, or if redness, irritation, swelling, pain, or other symptoms develop or increase. Keep out of reach of children In case of accidental ingestion, seek medical attention immediately.

Reported adverse events (FAERS/openFDA)#

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