Label: GINGICAINE GEL- gingicaine gel banana flavor gel

  • NDC Code(s): 10129-035-01, 10129-035-03, 10129-035-05
  • Packager: Gingi-Pak a Division of the Belport
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated December 8, 2021

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  • Active ingredient

    Active ingredients

  • Inactive ingredient

    Inactive ingredient

  • Precautions

    Precautions

  • Consult a doctor promptly

    Consult a doctor promptly

  • Allergy Alert and Contraindication

    ContraindicationsAllergy alert002

  • Purpose

    Purpose

  • Keep out of reach of children

    Keep out of reach of children

  • Dosage and Administration

    Dosage and Administration001Dosage and Administration002

  • Indications and Uses

    IndicationUses

  • Avoid excessive heat

    Avoid excessive heat

  • Warnings

    Warnings

  • GingiCaine Gel Banana label

    Jar Label

  • GingiCaine Gel Banana-Hakusui

    GingiCaine Gel Banana-Hakusui

  • INGREDIENTS AND APPEARANCE
    GINGICAINE GEL 
    gingicaine gel banana flavor gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10129-035
    Route of AdministrationORAL, DENTAL, PERIODONTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE200 mg
    Inactive Ingredients
    Ingredient NameStrength
    POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P) 260 mg
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) 520 mg
    POTASSIUM SODIUM SACCHARATE (UNII: 73U34YC90U) 20 mg
    Product Characteristics
    ColoryellowScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10129-035-031 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/06/1993
    2NDC:10129-035-056 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/06/1993
    3NDC:10129-035-011 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/07/2001
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart35607/06/1993
    Labeler - Gingi-Pak a Division of the Belport (008480121)