Label: LAUNCH MEDICAL- lidocaine hydrochloride cream

  • NDC Code(s): 54723-018-01
  • Packager: Sambria Pharmaceuticals, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 28, 2024

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  • Drug Facts

  • Active ingredient

    Lidocaine HCL 4.0% w/w

  • Purpose

    External Analgesic

  • Uses

    For temporary relief of pain and itching.

  • Warnings

    • For external use only. 
    • Avoid contact with eyes. 
    • Do not use in large quantities, particularly over raw surfaces or blistered areas. 
    • If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again with a few days, discontinue use of this product and consult a doctor. 
    • If product is swallowed get medical help or contact a Poison Control Center right away.
  • KEEP OUT OF REACH OF CHILDREN

  • Directions

    • Apply in a circular motion for 30 to 60 seconds over intact skin. 
    • For adults and children two-years and older, apply to affected area not more than 3 to 4 times daily. 
    • Children under 2 years of age consult a physician.
  • Inactive ingredients

    Arnica Montana Flower Extract, C13-14 Isoparaffin, Dimethyl Sulfone (MSM), Emu Oil, Ethoxydiglycol, Ethylhexylglycerin, Glucosamine Sulfate, Glycerin, Isopropyl Palmitate, Laureth-7, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Phenoxyethanol, Polyacrylamide, Propylene Glycol, Sodium Chondroitin Sulfate, Stearic Acid, Triethanolamine, Water

  • Other information

    Protect this product from excessive heat and direct sun. 

  • Questions?

    info@sambriapharma.com

    (888) 246-6601

  • Product label

    image description

  • INGREDIENTS AND APPEARANCE
    LAUNCH MEDICAL 
    lidocaine hydrochloride cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54723-018
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE4 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
    C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    EMU OIL (UNII: 344821WD61)  
    DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    LAURETH-7 (UNII: Z95S6G8201)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SODIUM CHONDROITIN SULFATE (PORCINE; 5500 MW) (UNII: H5BJH23Z9A)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54723-018-0130 mL in 1 JAR; Type 0: Not a Combination Product02/23/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01502/23/2024
    Labeler - Sambria Pharmaceuticals, LLC (078676259)
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