Label: TYLENOL PRECISE PAIN RELIEVING- lidocaine cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 13, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Lidocaine 4% ………………………………………. Topical analgesic

    Topical analgesic

  • Uses

    For the temporary relief of pain

  • Warnings

    • For external use only

    Do not use

    • in large quantities, particularly over raw surfaces or blistered areas

    When using this product

    • avoid contact with eyes

    Stop use and ask a doctor if

    • condition worsens or symptoms persist for more than 7 days
    • Symptoms clear up and occur again within a few days

    • Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
  • Directions

    • use only as directed
    • adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily
    • Children under 12 years of age: ask a doctor
  • Other Information

    • store at 15˚ to 30 ˚C (59 ˚ to 86 ˚F)
  • Inactive Ingredients

    carbomer copolymer, cetearyl olivate, cetyl alcohol, glycerin, isopropyl palmitate, phenoxyethanol, sodium polyacrylate, sorbitan olivate, water

  • Questions?

    call 1-877-895-3665 (toll-free) or 215-273-8755 (collect)

  • SPL UNCLASSIFIED SECTION

    Distributed by:

    JOHNSON & JOHNSON CONSUMER INC.

    Skillman, NJ 08558 USA

  • PRINCIPAL DISPLAY PANEL - 113 g Tube Carton

    ​Pain Relieving

    Cream

    Lidocaine 4%

    TYLENOL ®

    PRECISE TM

    Penetrating

    pain relief

    Targets pain

    receptor nerves

    Targets nerves

    to block

    pain signals

    Numbs away

    pain

    ROLLER BALL

    APPLICATOR

    Maximum Strength Lidocaine

    without a prescription

    FRAGRANCE FREE*

    For external

    use only

    NET WT 4.0 OZ (113 g)

    Tylenol

  • INGREDIENTS AND APPEARANCE
    TYLENOL PRECISE PAIN RELIEVING 
    lidocaine cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0795
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE40 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)  
    SORBITAN OLIVATE (UNII: MDL271E3GR)  
    CETEARYL OLIVATE (UNII: 58B69Q84JO)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69968-0795-41 in 1 CARTON07/03/2023
    1113 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01707/03/2023
    Labeler - Kenvue Brands LLC (118772437)
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