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Lidocaine HCL 4.0% w/w
2016-12-26 08:33:50 来源: 作者: 【 】 浏览:451次 评论:0
  • Active Ingredients

    Lidocaine HCL 4.0% w/w

    Purpose

    External Anesthetic

  • Uses

    For temporary relief of pain and itching due to minor skin irritation.

  • Warnings

    - For external use only.

    - Avoid contact with eyes.

  • DO NOT USE

    - ​Do not use ​in large quantities, particularly over raw surfaces or blistered areas.

  • STOP USE

    - ​Stop use and ask a doctor ​if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days.  Discontinue use.

  • KEEP OUT OF REACH OF CHILDREN

    - ​Keep out of reach of children.​  If product is swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    For adults and children two-years or older: Apply to affected area not more than 3 or 4 times daily.  Children under 2 years of age: consult a physician.

  • ​Inactive Ingredients

    Aqua (Deionized Water), Arnica Montana Floweri Extract, C13-14 Isoparaffin, Chondroitin Sulfate, Emu Oil, Ethoxydiglycol, Ethylhexylglycerin, Glucosamine Sulfate, Isopropyl Palmitate, Laureth-7, Melaleuca Alternifolia (Tea Tree) Oil, Methylsulfonylmenthane (MSM), Phenoxyethanol, Polyacrylamide, Propylene Glycol, Stearic Acid, Triethanolamine.

  • ​Other Information

    Protect this product from excessive heat and direct sun.

  • ​Questions or Comments?

    FDA Registered: NDC No 54723-175-22

    info@sambriapharma.com

  • INGREDIENTS AND APPEARANCE
    NEUROMED 7 TOPICAL PAIN RELIEF  lidocaine hydrochloride cream
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:54723-175
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 4 g  in 100 g
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
    C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
    SODIUM CHONDROITIN SULFATE (PORCINE; 5500 MW) (UNII: H5BJH23Z9A)  
    EMU OIL (UNII: 344821WD61)  
    DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)  
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    TROLAMINE (UNII: 9O3K93S3TK)  
     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:54723-175-22 1 in 1 CARTON 04/13/2016  
    1   63 g in 1 TUBE; Type 0: Not a Combination Product    
     
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part348 08/15/2013  
    Labeler - Sambria Pharmaceuticals, LLC (078676259)
    Establishment
    Name Address ID/FEI Business Operations
    A.I.G. Technologies, Inc.   171837367 manufacture(54723-175) 
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