Label: WILL RELIEVE- lidocaine lotion

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated July 13, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Lidocaine 4%

  • Purpose

    Topical Analgesic

  • Use

    temporary relief of pain

  • Warnings

    For external use only

    Do not use

    • 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

    • 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

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

    If pregnant or breastfeeding,

    • ask a healthcare professional before use

    Keep out of reach of children and pets

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

    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

    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

    WILL™
    PERFORM
    BY SERENA WILLIAMS

    FAST ACTING

    PAIN RELIEF
    LOTION
    lidocaine

    NET WT 3 OZ (85 g)

    PRINCIPAL DISPLAY PANEL - 85 g Bottle Carton
  • INGREDIENTS AND APPEARANCE
    WILL RELIEVE 
    lidocaine lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82630-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Lidocaine (UNII: 98PI200987) (Lidocaine - UNII:98PI200987) Lidocaine3.4 g  in 85 g
    Inactive Ingredients
    Ingredient NameStrength
    CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)  
    Alcohol (UNII: 3K9958V90M)  
    ANGELICA SINENSIS ROOT (UNII: B66F4574UG)  
    Arnica Montana Flower (UNII: OZ0E5Y15PZ)  
    Butylene Glycol (UNII: 3XUS85K0RA)  
    Medium-Chain Triglycerides (UNII: C9H2L21V7U)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    Coconut Oil (UNII: Q9L0O73W7L)  
    DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)  
    Polysorbate 60 (UNII: CAL22UVI4M)  
    Glycerin (UNII: PDC6A3C0OX)  
    HEPTYL UNDECYLENATE (UNII: W77QUB6GXO)  
    ISOAMYL COCOATE (UNII: 14OG46E98E)  
    ISODODECANE (UNII: A8289P68Y2)  
    NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    PHYTATE SODIUM (UNII: 88496G1ERL)  
    Water (UNII: 059QF0KO0R)  
    Product Characteristics
    ColorWHITEScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82630-001-011 in 1 CARTON08/01/2022
    185 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34808/01/2022
    Labeler - Will Perform, PBC (118584310)
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