Label: ANECREAM- lidocaine 4% cream

  • NDC Code(s): 24357-701-01, 24357-701-05, 24357-701-06, 24357-701-07, view more
    24357-701-15, 24357-701-30, 24357-701-50
  • Packager: Focus Health Group
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 12, 2024

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

  • Active Ingredient:

    Lidocaine 4% w/w

  • Purpose

    Topical anesthetic

  • Uses

    temporarily relieves pain and itching due to:

    • minor cuts
    • minor scrapes
    • sunburn
    • minor skin irritations
    • minor burns
    • insect bites
  • WARNINGS

    For external use only.

    When using this product

    • do not use in or near the eyes
    • do not use in large quantities, particularly over raw surfaces or blistered areas

    Stop use and ask doctor if

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

    Keep out of reach of children.

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

  • Directions

    • Adults and children 2 years and older: Apply externally to the affected area up to 3-4 times daily.
    • Children under 2 years of age: Consult a doctor.
  • Other Information

    Store at USP controlled room temperature 20-25 degC (68-77 deg.F).

  • Inactive ingredients

    benzyl alcohol, carbomer 940, cholesterol, hydrogenated lecithin, polysorbate 80, propylene glycol, tocopherol acetate, trolamine, water

  • Anecream 30g Tube

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

    Anecream Topical Anesthetic Cream

    Net. Wt. 30g

    Distributed by: Focus Health Group

    Knoxville, TN 37919

    781_30g

  • INGREDIENTS AND APPEARANCE
    ANECREAM 
    lidocaine 4% cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24357-701
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE4 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    WATER (UNII: 059QF0KO0R)  
    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)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:24357-701-301 in 1 CARTON06/01/2007
    130 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:24357-701-151 in 1 CARTON06/01/2007
    215 g in 1 TUBE; Type 0: Not a Combination Product
    3NDC:24357-701-075 in 1 CARTON06/01/2007
    3NDC:24357-701-055 g in 1 TUBE; Type 0: Not a Combination Product
    4NDC:24357-701-065 in 1 CARTON03/11/2011
    4NDC:24357-701-055 g in 1 TUBE; Type 0: Not a Combination Product
    5NDC:24357-701-5050 in 1 CARTON08/01/2020
    5NDC:24357-701-012.5 g in 1 PACKET; Type 0: Not a Combination Product
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01706/01/2007
    Labeler - Focus Health Group (826939949)
    Registrant - DSC Laboratories Inc. (097807374)
    Establishment
    NameAddressID/FEIBusiness Operations
    DSC Laboratories Inc.097807374manufacture(24357-701)