FDA.reportPublic FDA data

Will Relieve Roll-On

Manufacturer
Will Perform, PBC
Effective date
2023-07-13
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:55:40

Label at a glance#

ProductWill Relieve Roll-On
Active ingredientLidocaine Hydrochloride
Label structure9 sections

Dosage and administration

adults and children over 12 years: apply a thin layer 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 HCl 4%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Use

INDICATIONS & USAGE SECTION

temporary relief of pain

Warnings

WARNINGS SECTION

For external use only

Flammable

SPL UNCLASSIFIED SECTION

  • keep away from excessive heat or open flame

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:

  • apply a thin layer 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., aminomethyl propanol, angelica polymorpha sinensis root extract, arnica montana flower extract, bisabolol, caprylic/capric triglyceride, capryloyl glycerin/sebacic acid copolymer, diheptyl succinate, fragrance, glycerin, water

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL - 88 mL Bottle Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

WILL™
PERFORM
BY SERENA WILLIAMS

FAST ACTING

PAIN RELIEF
ROLL-ON
lidocaine

3 FL OZ (88 mL)

PRINCIPAL DISPLAY PANEL - 88 mL Bottle Carton
PRINCIPAL DISPLAY PANEL - 88 mL Bottle Carton

DailyMed Pharmacologic Classes#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
070fbed5-7088-434a-a7ce-f2a64d8d40acProduct name220260107
bee66ce1-adb7-9d3b-67d9-582e4c54e80fProduct name520250819
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
7d755fa1-1087-4dcd-98f0-6d4bba479a57Product name320210602
aed701d5-9c75-dfaf-7154-cde46179faeaProduct name920200313
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
49fa150c-f0de-cce7-3d9c-993ed81c5698Product name120140508
4d7ae718-ed00-bae8-2abe-9eaec1eef7ffProduct name120140508
9137811f-f279-8640-5aeb-99fa2145d64dProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82630-002-012025-01-30C16284748780-12cef2736-9b9f-d83d-e063-dadaa90ab31fWill Relieve™ Roll-On

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82630-002-01Will Relieve Roll-On88 mL in 1 BOTTLE, WITH APPLICATORGEL883
82630-002-01Will Relieve Roll-On1 in 1 CARTONGEL13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82630-002WILL RELIEVE ROLL-ON (LIDOCAINE HYDROCHLORIDE) GEL [WILL PERFORM, PBC]3Legacy NDC, 2 package rows20230720_24e1b335-dac2-4347-90e3-f7cce7459526.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82630-00282630-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
Lidocaine HydrochlorideV13007Z41AACTIR
Water059QF0KO0RIACT
CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED)809Y72KV36IACT
Alcohol3K9958V90MIACT
GlycerinPDC6A3C0OXIACT
Medium-Chain TriglyceridesC9H2L21V7UIACT
DIHEPTYL SUCCINATE057N7SS26YIACT
CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S)N7YC58165TIACT
LEVOMENOL24WE03BX2TIACT
ANGELICA SINENSIS ROOTB66F4574UGIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
Arnica Montana FlowerOZ0E5Y15PZIACT

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
b665f3a8-af0f-490c-b929-21cf48ab00a024e1b335-dac2-4347-90e3-f7cce74595262023-07-13WarningsExact identifier
spl id: b665f3a8-af0f-490c-b929-21cf48ab00a0
spl set id: 24e1b335-dac2-4347-90e3-f7cce7459526

Reported adverse events (FAERS/openFDA)#

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