Will Relieve™ Spray

Manufacturer
Will Perform, PBC
Effective date
2023-10-06
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:56:29

Label at a glance#

ProductWill Relieve
Active ingredientLidocaine
Label structure9 sections

Dosage and administration

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 does not need to be rubbed in children 12 years or younger: ask a doctor

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Use

INDICATIONS & USAGE SECTION

temporary relief of pain

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • on large areas of the body or on a cut, irritated or swollen 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. Read and follow all directions and warnings on this carton
  • do not allow contact with eyes and mucous membranes
  • do not bandage or apply local heat (such as heating pads) or medicated patch to the 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

  • conditions worsen
  • redness is present
  • irritation develops
  • symptoms persist for more than 7 days or clear up and occur again within a few days

Extremely Flammable

SPL UNCLASSIFIED SECTION

  • do not use near fire 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 120°F (49°C)

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding,

  • ask a healthcare professional before use

Keep out of reach of children and pets

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 over 12 years:

  • spray affected area every 6 to 8 hours, not to exceed 3 applications in a 24 hour period
  • product does not need to be rubbed in

children 12 years or younger:

  • ask a doctor

Inactive Ingredients

INACTIVE INGREDIENT SECTION

alcohol denat., angelica polymorpha sinensis root extract, arnica montana flower extract, caprylic/capric triglyceride, fragrance, glycerin, isobutane, propylene glycol, water

SPL UNCLASSIFIED SECTION

Distributed by Will Perform, PBC, 4040 Civic Center Drive, Suite 200, San Rafael, CA 94903

PRINCIPAL DISPLAY PANEL - 113 g Can Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

WILL™
PERFORM
BY SERENA WILLIAMS

FAST ACTING

PAIN RELIEF
SPRAY
lidocaine

NET WT 4 OZ (113 g)

PRINCIPAL DISPLAY PANEL - 113 g Can Carton
PRINCIPAL DISPLAY PANEL - 113 g Can Carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1869797lidocaine 4 % Topical SprayPSN3
1869797lidocaine 40 MG/ML Topical SpraySCD3
1869797lidocaine 4 % Topical SpraySY3

DailyMed Pharmacologic Classes#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82630-003-012025-01-30C16284748780-12cef2736-7579-d83d-e063-dadaa90ab31fWill Relieve™ Spray

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82630-003-01Will Relieve1 in 1 CARTONAEROSOL, SPRAY13
82630-003-01Will Relieve113 g in 1 CANAEROSOL, SPRAY1133

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82630-003WILL RELIEVE (LIDOCAINE) AEROSOL, SPRAY [WILL PERFORM, PBC]3Legacy NDC, 2 package rows20231007_f1de4a91-7cb9-4eb4-873d-16dcd233df90.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82630-00382630-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
20a8be4b-7234-42e5-9732-01111a985536f1de4a91-7cb9-4eb4-873d-16dcd233df902023-10-06WarningsExact identifier
spl id: 20a8be4b-7234-42e5-9732-01111a985536
spl set id: f1de4a91-7cb9-4eb4-873d-16dcd233df90

Reported adverse events (FAERS/openFDA)#

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