Quick Numb

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: Quick Numb
Generic name: LIDOCAINE
Manufacturer: Clinical Resolution Laboratory, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 351b95a6-e038-d9aa-e063-6294a90a4172
SPL ID: 364a4eb9-6ba7-b6bf-e063-6394a90aeeb2
Version: 3
Effective date: 2025-05-29
Source export date: 2026-09-28
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:25:48

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		Quick Numb	openfda.brand_name
generic name		LIDOCAINE	openfda.generic_name
manufacturer name		Clinical Resolution Laboratory, Inc.	openfda.manufacturer_name
ndc	package	63742-333-02	openfda.package_ndc
ndc	package	63742-333-01	openfda.package_ndc
ndc	product	63742-333	openfda.product_ndc
ndc11	package	63742033302	derived:openfda.package_ndc
ndc11	package	63742033301	derived:openfda.package_ndc
rxcui		1366789	openfda.rxcui
spl id		364a4eb9-6ba7-b6bf-e063-6394a90aeeb2	id
spl set id		351b95a6-e038-d9aa-e063-6294a90a4172	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) ■ 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. ■ Certain persons can develop allergic reactions to ingredients in this product. If the symptom being treated does not subside or if redness, irritation, swelling, pain, or other symptoms develop or increase, discontinue use and consult a doctor.

Reported adverse events (FAERS/openFDA)#

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