Label: WALGREENS PAIN RELIEVING CREAM- lidocaine 4% cream

  • NDC Code(s): 0363-3037-02, 0363-3037-04
  • Packager: Walgreens
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 31, 2023

If you are a consumer or patient please visit this version.

View All Sections
  • ACTIVE INGREDIENT

    Lidocaine HCl 4%

  • PURPOSE

    Topical Anesthetic

  • INDICATIONS & USAGE

    temporarily relieves minor joint and muscle pain

  • WARNINGS

    For external use only

  • DO NOT USE

    • On large areas of the body or on cut,irritated or swollen skin
    • On punctured wounds
    • for more than one week without consulting a doctor

  • WHEN USING

    • Use only as directed. Read and follow all directions and warnings on this carton
    • do not allow contact with eyes
    • do not bandage or apply local heat to the area of use
    • do not use at the same time as other topical analgesics
  • STOP USE

    • the condition worsens, redness present, irritation develops
    • symptoms persist for more than 7 days or clear up and occur again within a few days
  • PREGNANCY OR BREAST FEEDING

    ask a health professional before use

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children and pets

    If swallowed, get medical help or contact a Poison Control Center right way

  • DOSAGE & ADMINISTRATION

    Adults and children over 12 years: Apply a thin layer to the affected area every 6 to 8 hours, not exceeding 3 applications in a 24 hour period.

    Children under 12 years of age: ask a doctor

  • INACTIVE INGREDIENT

    benzyl alcohol, carbomer, glycerin, hydrogenated lecithin, isopropyl palmitate, polysorbate 80, triethanolamine, vitamin E, water

  • QUESTIONS

    1800-925-4733

  • PRINCIPAL DISPLAY PANEL

    Package Carton 2.7 ozPackage Carton 4.7 oz

  • INGREDIENTS AND APPEARANCE
    WALGREENS PAIN RELIEVING CREAM 
    lidocaine 4% cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-3037
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS4 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CARBOMER 940 (UNII: 4Q93RCW27E)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-3037-0276.5 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/10/2022
    2NDC:0363-3037-04133 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/10/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01703/10/2022
    Labeler - Walgreens (008965063)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!