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, PHENYLEPHRINE HYDROCHLORIDE
Manufacturer: Clinical Resolution Laboratory, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 65d3b614-361d-4fb9-9583-a95be754bc82
SPL ID: 353212d3-630c-14b4-e063-6394a90a5b29
Version: 5
Effective date: 2025-05-15
Source export date: 2026-10-12
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:31:32

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 · 12 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, PHENYLEPHRINE HYDROCHLORIDE	openfda.generic_name
manufacturer name		Clinical Resolution Laboratory, Inc.	openfda.manufacturer_name
ndc	package	63742-034-01	openfda.package_ndc
ndc	product	63742-034	openfda.product_ndc
ndc11	package	63742003401	derived:openfda.package_ndc
rxcui		2590656	openfda.rxcui
spl id		353212d3-630c-14b4-e063-6394a90a5b29	id
spl set id		65d3b614-361d-4fb9-9583-a95be754bc82	set_id
unii		98PI200987	openfda.unii
unii		04JA59TNSJ	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. avoid contact with the eyes. keep out of reach of children. Do not use this product if pregnant or breastfeeding, ask a health professional before use. seal is broken or missing. you have heart disease, high blood pressure, thyroid disease, diabetes, or difficulty in urination due to enlargement of prostate gland unless directed by a doctor. When using this product do not exceed the recommended daily usage. 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. if swallowed, call your Poison Control Center at 1(800) 222 1222. If condition worsens or does not improve within 7 days, consult a doctor. Stop use and ask a doctor if the symptom being treated does not subside, or redness, irritation, swelling, pain, or other symptoms develop or increase.

Reported adverse events (FAERS/openFDA)#

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