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Releev Cold Sore Treatment (Topical Pharmaceuticals Inc.)

Available Formats

Dosage Form Package Information Links
LIQUID 1 BOTTLE, DROPPER in 1 BLISTER PACK (15478-001-06) > 6 mL in 1 BOTTLE, DROPPER Label Information
LIQUID 1 POUCH in 1 BLISTER PACK (15478-001-01) > 1 BOTTLE, DROPPER in 1 POUCH > 1 mL in 1 BOTTLE, DROPPER Label Information
LIQUID 1 BOTTLE, DROPPER in 1 BLISTER PACK (15478-001-03) > 3 mL in 1 BOTTLE, DROPPER Label Information

Complete Releev Cold Sore Treatment Information

  • Active ingredients

    Benzalkonium chloride .13%


  • USE

    Treat cold sores/ fever blister. For the pain, tingling, itching, and the burning association with cold sore. May be used as an antiseptic to help cleases or dry cold sores, and fever blister.May be used inside the mouth on sores, and fever blister


  • Warnings

    Do not swallow.Do not use if allergic to Asteracea ( daisy) family flower. Do not use for yeast infections.May be used in conjunction with yeast infections. Uses only as directed. For external used only.Brief tingling may improve, contact a health care professional. Avoid contact with eyes. We suggest that you not used alcohol, during an outbreak, or when using this product.

    Keep this and all drug out of reach of children.


  • Directions

    Adult and children 2 years of age and older. Intended as a 1 day cold sore symptom treatment, apply Releev to clean dry affected area 3-4 times throughout the day by dabbing and pressing solution into area well.


  • INDICATIONS & USAGE

    Allow to dry.Best when used at first sign of outbreak. Do not use applicator. do to the natural ingredients in this product color may vary. Product dries clear.

  • INACTIVE INGREDIENT

    Purified water, Viracea Proprietary Echinacea herb extract, Methyl cellusose, Methyl Paraben, Potassium sorbate, Propyl Paraben.


  • PRINCIPAL DISPLAY PANEL

    releev carton

    1cc carton3cc carton6ml carton


  • INGREDIENTS AND APPEARANCE
    RELEEV COLD SORE TREATMENT 
    benzalkonium chloride liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:15478-001
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Benzalkonium Chloride (UNII: F5UM2KM3W7) (Benzalkonium - UNII:7N6JUD5X6Y) Benzalkonium Chloride 1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    Water (UNII: 059QF0KO0R)  
    HYPROMELLOSE 2910 (4000 MPA.S) (UNII: RN3152OP35)  
    Methylparaben (UNII: A2I8C7HI9T)  
    Potassium Sorbate (UNII: 1VPU26JZZ4)  
    Propylparaben (UNII: Z8IX2SC1OH)  
    Echinacea purpurea flowering top (UNII: 2EMS3QFX65)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:15478-001-01 1 in 1 BLISTER PACK
    1 1 in 1 POUCH
    1 1 mL in 1 BOTTLE, DROPPER
    2 NDC:15478-001-03 1 in 1 BLISTER PACK
    2 3 mL in 1 BOTTLE, DROPPER
    3 NDC:15478-001-06 1 in 1 BLISTER PACK
    3 6 mL in 1 BOTTLE, DROPPER
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 06/01/2006
    Labeler - Topical Pharmaceuticals Inc. (831530683)