Label: ANECREAM 5- lidocaine 5% cream

  • NDC Code(s): 24357-702-15, 24357-702-30
  • Packager: Focus Health Group
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 12, 2024

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  • Active Ingredient:

    Lidocaine 5% w/w

  • Purpose


    Local anesthetic

  • Uses

    temporarily relieves pain and itching due to anorectal disorders

  • Warnings


    When using this product

    • avoid contact with eyes
    • do not exceed recommended dosage unless directed by a doctor

    Stop and ask a doctor if

    • rectal bleeding occurs
    • condition worsens or does not improve within 7 days
    • allergic reaction occurs
    • redness, irritation, swelling, pain or other symptoms begin or increase
    • symptoms clear up and return within a few days

    Keep out of reach of children.

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

  • Directions

    • When practical, clean area with mild soap and warm water and rinse thoroughly. Gently dry by patting of blotting with toilet tissue or soft cloth before applying.
    • Adults and children 12 years and older: Apply to the affected area up to 6 times a day.
    • Children under 12 years of age: Consult a doctor.
  • Other information

    Store at USP controlled room temperature 20-25C (66-77F).

  • Inactive ingredients

    benzyl alcohol, carbomer 940, cholesterol, hydrogenated lecithin, isopropyl myristate, polysorbate 80, propylene glycol, tocopheryl acetate, trolamine, water.


  • Anecream5 15g Tube Carton

    Anecream 5 15g

    AC 5art 15gm.jpg

    The product package shown above represents a sample of that currently in use. Additional packaging may also be available.

    Anecream5 Anorectal Cream

    Net. Wt. 15g

    Distributed by: Focus Health Group

    Knoxville, TN 37919

    Anecream5 15g Tube Carton

  • INGREDIENTS AND APPEARANCE
    ANECREAM 5 
    lidocaine 5% cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24357-702
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE5 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)  
    CHOLESTEROL (UNII: 97C5T2UQ7J)  
    LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:24357-702-151 in 1 CARTON12/20/2011
    115 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:24357-702-301 in 1 CARTON05/21/2019
    230 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00712/20/2011
    Labeler - Focus Health Group (826939949)
    Registrant - DSC Laboratories Inc. (097807374)
    Establishment
    NameAddressID/FEIBusiness Operations
    DSC Laboratories, Inc.097807374manufacture(24357-702)
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