Label: 3X MEDICATED TOOTHACHE AND GUM GEL- benzocaine gel

  • 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 May 6, 2020

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

  • ACTIVE INGREDIENT

    Acive Ingredients Purpose

    Benzocaine 20% .......... Oral Pain Reliever

    Menthol 0.26% ............. Oral Pain Reliever

    Zinc Chloride 0.15% .... Oral Astringent

  • Use

    Use * for the temporary relief of pain due to minor irritation or injury of the mouth and gums

  • INDICATIONS & USAGE

    Methemoglobinemia warning: use of this product may cause methemoglobinema, a serious condition that must be treated promptly because it reduces the amount of oxygen in the blood. This can occur even if you have used this prouct before. Stop use and seek immediate medical attention if you or a child in your care develops: * pale, gray, or blue colored skin (cyanosis) * headache * rapid heart rate * shortness of breath * dizziness or lightheadedness * fatigue or lack of energy

    Allergy Alert

    do not use this product if you have a history of allergy to local anesthetics such as procaine, butacaine, benzocaine or other "caine" anesthetics

    Do not use * more than directed * for more than 7 days unless told to do so by a dentist or doctor * for teething * in children under 2 years of age

    Stop use and ask a doctor if * swelling, rash or fever develops * irritation, pain or redness persists or worsens * symptoms do not improve in 7 days * allergic reaction occurs

    Keep out of reach of children In case of overdose, get medical help or contact a Poison Control Center right away.

  • Directions

    Directions * cut open tip of tube on score mark * do not use if tip is cut prior to opening * adults adn children 2 years of age and older: apply to affected area up to 4 times daily or as directed by a dentist or doctor * children under 12 years of age should be supervised in the use of this product * children under 2 years of age: do not use

  • OTHER SAFETY INFORMATION

    Other information * do not use if tip is cut prior to opening * this preparation is intended for use in cases of toothache, only as a temporary expedient until a dentist can be consulted * do not use continuously ( this formula will stay in place for extended duration of relief * avoid using toothpaste or drinking soft drinks or fruit juices for at least one hour after applying

  • INACTIVE INGREDIENT

    Inactive ingredients ammonium glycyrrhizate, favor, PEG-8, PEG-75, sodium saccharin, sorbic acid

  • PRINCIPAL DISPLAY PANEL

    Full artworkToothache and Gum Reliever

    20% benzocaine to relive oral pain

    Astringent to help prevent infection

    Menthol to soothe gums

    3x medicated

    oral pain reliever/astringent

    Net Wt 0.42 oz (11.9 g)

  • INGREDIENTS AND APPEARANCE
    3X MEDICATED TOOTHACHE AND GUM GEL 
    benzocaine gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-0613
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE20 g  in 100 g
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.26 g  in 100 g
    ZINC CHLORIDE (UNII: 86Q357L16B) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION0.15 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    SORBIC ACID (UNII: X045WJ989B)  
    AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C)  
    Product Characteristics
    Colorwhite (Cloudy white to beige) Score    
    ShapeSize
    FlavorMINTImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11822-0613-91 in 1 CARTON05/06/2020
    111.7 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart35605/06/2020
    Labeler - Rite Aid (014578892)
    Establishment
    NameAddressID/FEIBusiness Operations
    Lornamead080046418manufacture(11822-0613)