Label: ICEQUAKE LIDOCAINE ANALGESIC- lidocaine hydrochloride liquid

  • NDC Code(s): 69822-430-03
  • Packager: Southern Sales & Service, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 29, 2023

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  • Drug Facts

  • Active ingredient

    Lidocine HCl 4%

  • Purpose

    Topical anesthetic

  • Use

    Temporarily relieves minor pain

  • Warnings

    For external use only

    Do not use

    • on large areas of the body or on 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 label.
    • do not allow contact with the eyes
    • do not bandage or apply local heat (such as heating pads) to area of use
  • Do not use

    • on large areas of the body or on cut, irritatred or swollen skin
    • on puncture wounds
    • for more than one week without consulting a doctor
  • condition worsens Stop use and ask a doctor if

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

    keep away from fire or flame

  • If pregnant or breast-feeding

    ask a health 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:

    apply a thin layer to 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

    Disodium EDTA, isopropyl alcohol, glycerin, methylparaben, polysorbate 20, propylparaben, purified water, xanthan gum.

  • IceQuake Lidocaine Topical Analgesic Liquid 74ml

    front labelfacts panel

  • INGREDIENTS AND APPEARANCE
    ICEQUAKE LIDOCAINE ANALGESIC 
    lidocaine hydrochloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69822-430
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS4 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    WATER (UNII: 059QF0KO0R)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69822-430-0374 mL in 1 BOTTLE; Type 0: Not a Combination Product08/01/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01708/01/2022
    Labeler - Southern Sales & Service, Inc. (013114906)
    Registrant - Southern Sales & Service, Inc. (013114906)
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