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VenomX (Phillips Company)

Available Formats

Dosage Form Package Information Links
LIQUID 1 BOTTLE, DROPPER in 1 BOTTLE, PLASTIC (43074-207-02) > 3 mL in 1 BOTTLE, DROPPER (43074-207-01) Label Information

Complete VenomX Information

  • DRUG FACTS

    Questions and Side effects
    Use of this product results in no known side effects when used according to directions. Phillips Company, 311 Chickasaw Street, Millerton, OK USA 74750; Tel. 580-746-2430
    Email address: hp@valliant.net


  • ACTIVE INGREDIENTS

    Active Ingredients                            Purpose
    Zinc acetate (.1% by volume)           Skin Protectant


  • ASK DOCTOR

    Ask a doctor
    If symptoms last for more than 7 days or clear up and recur within a few days.
    If the conditions do not improve.  
    Before use on children under 2 years.
    Before use if you are allergic to any ingredients listed on this label.


  • DO NOT USE


    Warnings
    For external use only   
    Keep away from children   
    Avoid contact with eyes  
    May be harmful if swallowed or inhaled


  • CHILDREN

     
    Keep away from children   
    Avoid contact with eyes  
    May be harmful if swallowed or inhaled


  • PURPOSE


    Active Ingredients                            Purpose
    Zinc acetate (.1% by volume)           Skin Protectant


  • STOP USE


    If symptoms last for more than 7 days or clear up and recur within a few days.
    If the conditions do not improve.   
    Before use on children under 2 years.
    Before use if you are allergic to any ingredients listed on this label.
  • WHEN USING


    For external use only   
    Avoid contact with eyes  
    May be harmful if swallowed or inhaled
    If symptoms last for more than 7 days or clear up and recur within a few days.
    If the conditions do not improve.  
    Store at 40 to 120 degrees F.


  • WARNINGS



    Warnings
    For external use only
    Keep away from children
    Avoid contact with eyes
    May be harmful if swallowed or inhaled
    Use of this product results in no known side effects when used according to directions.

    Phillips Company, 311 Chickasaw Street, Millerton, OK USA 74750; Tel. 580-746-2430
    Email address: hp@valliant.net


  • DOSAGE & ADMINISTRATION

    Uses
    Temporarily protects injured or exposed skin or mucous membrane surfaces from harmful or annoying stimuli and may help provide relief to such surfaces

    Directions
    Apply to affected skin area and rub gently.  Repeat the process as needed.


  • USE

    Uses
    Temporarily protects injured or exposed skin or mucous membrane surfaces from harmful or annoying stimuli and may help provide relief to such surfaces

    Apply to affected skin area and rub gently.  Repeat the process as needed.


  • INACTIVE INGREDIENTS

    Inactive ingredients
    Water, color, glycerin, hydroxethylcellulose, chlor-hexidine gluconate, glucono delta lactone, methylparaben, sodium hydroxide,sodium dodecylbenzene sulfonate, dimethyl sulfoxide, witch hazel, ascorbic acid, magnesium stearate, silica and stearic acid. 


  • Image of product

    Image of product

    Image of product


  • INGREDIENTS AND APPEARANCE
    VENOMX 
    zinc acetate liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:43074-207
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    zinc acetate (UNII: FM5526K07A) (zinc - UNII:J41CSQ7QDS) zinc 0.001 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    dimethyl sulfoxide (UNII: YOW8V9698H)  
    ascorbic acid (UNII: PQ6CK8PD0R)  
    dipropylene glycol (UNII: E107L85C40)  
    water (UNII: 059QF0KO0R)  
    glycerin (UNII: PDC6A3C0OX)  
    chlorhexidine gluconate (UNII: MOR84MUD8E)  
    calcium gluconate (UNII: SQE6VB453K)  
    methylparaben (UNII: A2I8C7HI9T)  
    sodium hydroxide (UNII: 55X04QC32I)  
    sorbic acid (UNII: X045WJ989B)  
    magnesium stearate (UNII: 70097M6I30)  
    stearic acid (UNII: 4ELV7Z65AP)  
    witch hazel (UNII: 101I4J0U34)  
    sodium dodecylbenzenesulfonate (UNII: 554127163Y)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:43074-207-02 1 in 1 BOTTLE, PLASTIC
    1 NDC:43074-207-01 3 mL in 1 BOTTLE, DROPPER
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part347 08/23/2010
    Labeler - Phillips Company (612368238)
    Establishment
    Name Address ID/FEI Business Operations
    Phillips Company 612368238 manufacture