Label: THERA PLUS MAXIMUM STRENGTH FEMININE ANTI-ITCH- benzocaine, resorcinol cream

  • NDC Code(s): 80684-142-00
  • Packager: FOURSTAR GROUP USA, INC.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 26, 2025

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  • Drug Facts

  • Active ingredients

    Benzocaine 20%
    Resorcinol 3%

    Purpose

    External Analgesic

  • Uses

    temporarily relieves itching

  • Warnings

    For external use only.

    When using this product

    avoid contact with the eyes.

    Stop use and ask a doctor

    if condition worsens, or if symptoms persists for more than 7 days or clear up and occur again within a few days.

    Do not applyover large areas of the body.

    Keep out of reach of children.

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

  • Directions

    • Adults and children 12 years and older:apply a fingertip amount (approximately 1 inch strip) to the affected area not more than 3 to 4 times daily.
    • Children under 12 years:ask a doctor.
  • Other information

    Store at 20° - 25° C (68° - 77° F).

  • Inactive ingredientsa

    aloe barbadensis leaf juice, cetyl alcohol, cholecalciferol, edetate disodium, fragrance, glyceryl monostearate, isopropyl myristate, isopropyl palmitate, lanolin, methylparaben, mineral oil, petrolatum, propylene glycol, retinol, sodium lauryl sulfate, sodium sulfite, tocopherol, water

  • Package Labeling:

    Outer Package

  • INGREDIENTS AND APPEARANCE
    THERA PLUS MAXIMUM STRENGTH FEMININE ANTI-ITCH 
    benzocaine, resorcinol cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80684-142
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE200 mg  in 1 g
    RESORCINOL (UNII: YUL4LO94HK) (RESORCINOL - UNII:YUL4LO94HK) RESORCINOL30 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    CHOLECALCIFEROL (UNII: 1C6V77QF41)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    LANOLIN (UNII: 7EV65EAW6H)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    RETINOL (UNII: G2SH0XKK91)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    SODIUM SULFITE (UNII: VTK01UQK3G)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80684-142-0028 g in 1 TUBE; Type 0: Not a Combination Product02/26/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01702/26/2025
    Labeler - FOURSTAR GROUP USA, INC. (140099503)
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