Label: BASE LABORATORIES LIDOCAINE ANESTHETIC PAIN RELIEF- lidocaine cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 21, 2024

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  • Drug Facts

  • Active Ingredients

    Lidocaine 4%

    Purpose

    Topical Analgesic

  • Indications:

    Temporary relieves minor pain

  • Warnings:

    For external use only

    • Avoid contact with the eyes.
    • If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a physician 
    • Do not apply to wounds or damaged skin.
    • Do not bandage tightly.

    Do not use

    • in large quantities, particularly over raw surfaces or blistered areas.

    Keep out of reach of children 

    to avoid accidental ingestion!

    If swallowed, get medical help or contact the poison control center immediately.

  • 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: consult a doctor 
  • Other information:

    Store at 20 to 25 C (68 to 77 F)

  • Inactive Ingredients:

    Hemp Seed Oil, Aloe Vera Extract, Chamomile Extract, Glycerol, Cetearyl Alcohol, Cetearyl Glucoside, Propylene Glycol, Laurocapram, Stearic Acid, Glyceryl Stearate, PEG-100, EDTA, Cetyl Alcohol, Triethanolamine, Water

  • Package Labeling:

    Tube0

  • INGREDIENTS AND APPEARANCE
    BASE LABORATORIES LIDOCAINE ANESTHETIC PAIN RELIEF 
    lidocaine cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80327-010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE40 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CHAMOMILE (UNII: FGL3685T2X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    LAUROCAPRAM (UNII: 1F3X9DRV9X)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    POLYETHYLENE GLYCOL 4500 (UNII: TVH7653921)  
    EDETIC ACID (UNII: 9G34HU7RV0)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80327-010-601 in 1 CARTON08/31/2022
    160 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01708/31/2022
    Labeler - Joonem LLC (117633878)
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