CVS Maximum Strength LIDOCAINE PLUS

Manufacturer
CVS Pharmacy Inc.
Effective date
2023-11-26
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:02:46

Label at a glance#

ProductCVS Maximum Strength LIDOCAINE PLUS
Active ingredientBENZYL ALCOHOL, LIDOCAINE HYDROCHLORIDE
Label structure9 sections

Indications and uses

For temporary relief of pain

Dosage and administration

Adults and children 12 years of age and over: spray to affected area not more than 3 to 4 times daily Children under 12 years of age: consult a doctor

Storage and handling

Avoid storing product in direct sunlight Protect product from excessive moisture Store with lid closed tighly

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzyl alcohol  10%

Lidocaine HCl  4%

Purpose

OTC - PURPOSE SECTION

Topical anesthetic

Uses

INDICATIONS & USAGE SECTION

For temporary relief of pain

Warnings

WARNINGS SECTION

For external use only

Flammable:

SAFE HANDLING WARNING SECTION

Keep away from fire or flame

-Do not use near heat or flame or while smoking.

-avoid long term storage above 40 degree Celcius.

-do not puncture or incinerate. COntents under pressure

-do not store at temperatures above 49 degree Celcius

Do not use

OTC - DO NOT USE SECTION

  • on large areas of the body or cut or wounds or damaged skin
  • on puncture wounds
  • for more than one week without consulting a doctor

When using this product

OTC - WHEN USING SECTION

  • use only as directed
  • avoid contact with the eyes, mucous membranes or rashes
  • avoid spraying on face
  • avoid inhalation of spray
  • do not bandage or apply local heat such as heating pads or a medicated patch to area of use
  • do not use at the same time as other topical analgesics

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • skin reactions occur, such as rash, itching, redness, irritaion, pain, swelling and blistering
  • conditions worsen
  • symptoms persist for more than 7 days
  • symptoms clear up and occur again within a few days

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years of age and over:

  • spray to affected area not more than 3 to 4 times daily

Children under 12 years of age:

consult a doctor

Other information

STORAGE AND HANDLING SECTION

  • Avoid storing product in direct sunlight
  • Protect product from excessive moisture
  • Store with lid closed tighly

Inactive ingredients

INACTIVE INGREDIENT SECTION

alcohol denatured, arnica montana flower extract, calendula officinalis flower extract, camellia sinensis leaf extract, chamomilla recutita (matricaria) flower extract , dimethyl sulfone (msm), Echinacea angustifolia extract, ilex paraguariensis leaf extract, isopropyl myristate, juniperus communis fruit extract, purified water 

Questions or comments?

OTC - QUESTIONS SECTION

Toll free 1-888-547-5492

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LidoLido

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2369354benzyl alcohol 10 % / lidocaine HCl 4 % Topical SprayPSN4
2369354benzyl alcohol 0.1 ML/ML / lidocaine hydrochloride 40 MG/ML Topical SpraySCD4
2369354benzyl alcohol 10 % / lidocaine HCl 4 % Topical SpraySY4

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
BENZYL ALCOHOL Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
LIDOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
332d03e4-aa24-4b11-841a-02bf41081920Product name120171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69842-573-63CVS Maximum Strength LIDOCAINE PLUS1 in 1 BOXSPRAY14
69842-573-63CVS Maximum Strength LIDOCAINE PLUS85 g in 1 TUBESPRAY854

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69842-573CVS MAXIMUM STRENGTH LIDOCAINE PLUS (BENZYL ALCOHOL, LIDOCAINE HYDROCHLORIDE) SPRAY [CVS PHARMACY INC.]4Current NDC, Legacy NDC, 2 package rows20231128_e6aff579-affb-41bb-8e36-53ea484cb0c5.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69842-57369842-573-63

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Source Document#

Source XML · Source PDF

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CVS Maximum Strength LIDOCAINE PLUSBENZYL ALCOHOL, LIDOCAINE HYDROCHLORIDECVS Pharmacy Inc.e6aff579-affb-41bb-8e36-53ea484cb0c52023-11-26WarningsExact identifier
ndc (package): 69842-573-63
ndc (product): 69842-573
ndc11 (package): 69842057363
spl id: 0b18b264-b5a9-74b9-e063-6394a90aba9a
spl set id: e6aff579-affb-41bb-8e36-53ea484cb0c5

Reported adverse events (FAERS/openFDA)#

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