Pain relieving lidocaine 4% dry spray

Manufacturer
Walgreens
Effective date
2023-10-31
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:58:41

Label at a glance#

ProductWalgreens pain relieving
Active ingredientLIDOCAINE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%

OTC - PURPOSE SECTION

Topical anesthetic

INDICATIONS & USAGE SECTION

temporarily relieves minor joint and muscle pain

WARNINGS SECTION

For External use only

OTC - DO NOT USE SECTION

Do not use

on large areas of the body or on cut, irritated or swollen skin

on puncture wounds

for more than one week without consulting a doctor

Extremely Flammable

do not use near heat or flame or while smoking

avoid long term storage above 104° F (40°C)

do not puncture or incinerate. Contents under pressure.

do not store at temperatures above 120F (49°C)

OTC - WHEN USING SECTION

When using this product

use only as directed. Read and follow all directions and warnings on this label.

do not allow contact with the eyes and mucous membranes

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

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

if swallowed, get medical help or contact Poison Control Center Right Away

OTC - STOP USE SECTION

Stop use and ask a doctor if

condition worsens

redness is present

irritation develops

symptoms persist for more than 7 days or clear up and occur again within few days

DOSAGE & ADMINISTRATION SECTION

adults and children over 12 years :

spray affected area every 6 to 8 hours, not to exceed 3 applications in a 24 hour period

product wil dry quickly on its own, and does not need to be rubbed in

children 12 years or younger: ask a doctor

INACTIVE INGREDIENT SECTION

caprylic/capric triglyceride, isobutane, propylene glycol, SD alcohol 40 B (30%)

OTC - QUESTIONS SECTION

1-800-925-4733

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1869797lidocaine 4 % Topical SprayPSN4
1869797lidocaine 40 MG/ML Topical SpraySCD4
1869797lidocaine 4 % Topical SpraySY4

DailyMed Pharmacologic Classes#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-3038-04Walgreens pain relieving113 g in 1 BOTTLE, SPRAYAEROSOL, SPRAY1134

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-3038WALGREENS PAIN RELIEVING (LIDOCAINE 4%) AEROSOL, SPRAY [WALGREENS]4Current NDC, Legacy NDC, 1 package rows20231102_ce2b9e57-749d-715c-e053-2995a90aaf8d.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-30380363-3038-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML

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
Walgreens pain relievingLIDOCAINE 4%Walgreensce2b9e57-749d-715c-e053-2995a90aaf8d2023-10-31WarningsExact identifier
ndc (package): 0363-3038-04
ndc (product): 0363-3038
ndc11 (package): 00363303804
spl id: 09057091-4886-4fae-e063-6294a90a95e5
spl set id: ce2b9e57-749d-715c-e053-2995a90aaf8d

Reported adverse events (FAERS/openFDA)#

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