FDA.reportPublic FDA data

Will Relieve™ Lotion

Manufacturer
Will Perform, PBC
Effective date
2023-07-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:55:42

Label at a glance#

ProductWill Relieve
Active ingredientLidocaine
Label structure9 sections

Dosage and administration

adults and children over 12 years: squeeze bottle and apply a thin layer of lotion over the affected area every 6 to 8 hours, not to exceed 3 applications in a 24 hour period 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

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding,

  • ask a healthcare professional before use

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children and pets

  • if swallowed, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

adults and children over 12 years:

  • squeeze bottle and apply a thin layer of lotion over the affected area every 6 to 8 hours, not to exceed 3 applications in a 24 hour period

children 12 years or younger:

  • ask a doctor

Inactive Ingredients

INACTIVE INGREDIENT SECTION

acrylates/c10-30 alkyl acrylate crosspolymer, alcohol denat., angelica polymorpha sinensis root extract, arnica montana flower extract, butylene glycol, caprylic/capric triglyceride, caprylyl glycol, cetearyl alcohol, cetyl alcohol, cocos nucifera (coconut) oil, ethoxydiglycol, fragrance, glycerin, heptyl undecylenate, isoamyl cocoate, isododecane, neopentyl glycol diheptanoate, phenoxyethanol, polysorbate 60, silica, sodium hyaluronate, sodium phytate, water

SPL UNCLASSIFIED SECTION

Distributed by Will Perform, PBC, 570 Pacific Ave., San Francisco, CA 94133

PRINCIPAL DISPLAY PANEL - 85 g Bottle Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

WILL™
PERFORM
BY SERENA WILLIAMS

FAST ACTING

PAIN RELIEF
LOTION
lidocaine

NET WT 3 OZ (85 g)

PRINCIPAL DISPLAY PANEL - 85 g Bottle Carton
PRINCIPAL DISPLAY PANEL - 85 g Bottle Carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2599519lidocaine 4 % Topical LotionPSN2
2599519lidocaine 40 MG/ML Topical LotionSCD2
2599519lidocaine 4 % Topical LotionSY2

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
82630-001-012025-01-30C16284748780-12cef2736-b48a-d83d-e063-dadaa90ab31fWill Relieve™ Lotion

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82630-001-01Will Relieve85 g in 1 BOTTLE, WITH APPLICATORLOTION852
82630-001-01Will Relieve1 in 1 CARTONLOTION12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82630-001WILL RELIEVE (LIDOCAINE) LOTION [WILL PERFORM, PBC]2Legacy NDC, 2 package rows20230722_da3504c3-b8fe-4836-ac41-4caff0448f64.zip

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82630-00182630-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

Name, UNII, Kind table
NameUNIIKind
Lidocaine98PI200987ACTIB
CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED)809Y72KV36IACT
Alcohol3K9958V90MIACT
ANGELICA SINENSIS ROOTB66F4574UGIACT
Arnica Montana FlowerOZ0E5Y15PZIACT
Butylene Glycol3XUS85K0RAIACT
Medium-Chain TriglyceridesC9H2L21V7UIACT
CAPRYLYL GLYCOL00YIU5438UIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
CETYL ALCOHOL936JST6JCNIACT
Coconut OilQ9L0O73W7LIACT
DIETHYLENE GLYCOL MONOETHYL ETHERA1A1I8X02BIACT
Polysorbate 60CAL22UVI4MIACT
GlycerinPDC6A3C0OXIACT
HEPTYL UNDECYLENATEW77QUB6GXOIACT
ISOAMYL COCOATE14OG46E98EIACT
ISODODECANEA8289P68Y2IACT
NEOPENTYL GLYCOL DIHEPTANOATE5LKW3C543XIACT
PHENOXYETHANOLHIE492ZZ3TIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
HYALURONATE SODIUMYSE9PPT4THIACT
PHYTATE SODIUM88496G1ERLIACT
Water059QF0KO0RIACT

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
e11f08b2-f8ea-40e4-b865-9fa3a31399b4da3504c3-b8fe-4836-ac41-4caff0448f642023-07-13WarningsExact identifier
spl id: e11f08b2-f8ea-40e4-b865-9fa3a31399b4
spl set id: da3504c3-b8fe-4836-ac41-4caff0448f64

Reported adverse events (FAERS/openFDA)#

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