Label: TYLENOL PRECISE WARMING PAIN RELIEVING- lidocaine cream

  • NDC Code(s): 69968-0794-4
  • Packager: Johnson & Johnson Consumer Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 13, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Lidocaine 4%

    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 0 to 30 0 C (59 0 to 86 0 F)

  • Inactive Ingredients

    carbomer copolymer, cetearyl olivate, cetyl alcohol, fragrance, glycerin, isopropyl palmitate, phenoxyethanol, sodium polyacrylate, sorbitan olivate, vanillyl butyl ether, 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

    Warming †

    Pain Relieving Cream

    Lidocaine 4%

    TYLENOL ®

    PRECISE TM

    Fast acting †

    Targeted

    penetrating

    pain relief

    ROLLER BALL

    APPLICATOR

    Maximum Strength Lidocaine

    without a prescription

    LIGHTLY SCENTED

    For external

    use only

    NET WT 4.0 OZ (113 g)

    Tylenol_01

  • INGREDIENTS AND APPEARANCE
    TYLENOL PRECISE WARMING PAIN RELIEVING 
    lidocaine cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0794
    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
    CETEARYL OLIVATE (UNII: 58B69Q84JO)  
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    VANILLYL BUTYL ETHER (UNII: S2ULN37C9R)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)  
    SORBITAN OLIVATE (UNII: MDL271E3GR)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69968-0794-41 in 1 CARTON02/12/2024
    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 DrugM01702/12/2024
    Labeler - Johnson & Johnson Consumer Inc. (118772437)
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