Label: GREENCAINE BLAST- lidocaine gel

  • NDC Code(s): 69747-040-01
  • Packager: ALMA Laboratories, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 12, 2023

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  • Drug Facts

    Lidocaine 4%

  • Active Ingredient

    Lidocaine 4%

    Purpose

    Topical Anesthetic

  • Uses

    For the temporary relief of pain and itching associated with minor skin irritations, minor cuts, minor burns, scrapes or insect bites.

  • Warnings

    For external use only

    Flammable

    Keep away from heat, sparks, electrical, fire or flame.

    When using this product

    avoid contact with the eyes.  Do not use in large quantities, particularly over raw surfaces or blistered areas.

    Stop use and ask a doctor

    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.

    Keep out of the reach of children

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

  • Directions

    Adults and children 2 years of age and older: Apply to affected  area not more than 3 to times daily. Children under 2 years of age consult a doctor.

  • Inactive ingredients:

    Aloe barbadensis leaf juice (aloe vera), caprylyl glycol, carbomer, disodium EDTA, glycerin, glyceryl laurate, jojoba oil, SD alcohol 40-B, trithanolamine, water.

  • Questions:

    Call  or visit (888) 306-6933www.greencaine.com

  • Package Labeling

    Label 1Label 2

  • INGREDIENTS AND APPEARANCE
    GREENCAINE BLAST 
    lidocaine gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69747-040
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE40 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GLYCERYL LAURATE (UNII: Y98611C087)  
    JOJOBA OIL (UNII: 724GKU717M)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69747-040-01113 g in 1 TUBE; Type 0: Not a Combination Product01/18/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01701/18/2018
    Labeler - ALMA Laboratories, Inc. (012180032)
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