Label: PRECAINE B CHOCOLATE VANILLA- benzocaine topical anesthetic gel

  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated January 22, 2020

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

  • Directions:

    Application Directions:

    For topical use only.

    For best results apply to previously dried oral mucosa with cotton swab or similar applicator for adquate control of pain.

    Removal of excess saliva during application minimizes dilution of the anesthetic and permits maximum penetration.

    Not more than 1.2 mg per Kg body weight per patient should be applied during a 24 hour period.

  • Warnings

    Recommended dosage should not be exceeded due to possible side effects.

    Keep out of the reach of children.

    For professional use only.

    Do not use in the eyes.

    Avoid swallowing.

    Not for home or unsupervised consumer use.

    Not for use on children 2 and younger or pregnant or nursing women.

  • Contraindications

    Precaine B is contraindicated in patients with known hypersensitivity to benzocaine or PABA.

  • Other Information

    For product SDS information, please go to www.pascaldental.com or contact Pascal directly.

    Store product between 60 degress F (16 degrees C) and 86 degrees F (30 degrees C)

    Rx only in USA

    Made in USA

  • Precaine B Chocolate Vanilla

    Precaine B LabelPrecaine B

    Topical Anesthetic Gel for oral use

    Chocolate Vanilla

    Contains: Benzocaine 20% in a flavored aqueous base

    Net contents: 30g

    Pascal International

    2929 Northup Way

    Bellevue, WA 98004

    425-827-4694

    REF 15-365

    SN72508/0217

  • INGREDIENTS AND APPEARANCE
    PRECAINE B CHOCOLATE VANILLA 
    benzocaine topical anesthetic gel
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:10866-0089
    Route of AdministrationDENTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE221 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    CARBOMER 934 (UNII: Z135WT9208) 125 mg  in 1 g
    Product Characteristics
    ColorgreenScore    
    ShapeSize
    FlavorVANILLA, CHOCOLATEImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10866-0089-130 g in 1 JAR; Type 0: Not a Combination Product08/16/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other08/16/2017
    Labeler - Pascal Company, Inc. (009260217)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pascal Company, Inc.009260217manufacture(10866-0089)