Label: LIDOSOLVE PAIN RELIEF- lidocaine hydrochloride liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 11, 2023

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  • Drug Facts

  • Active ingredients

    Lidocaine HCL 4.00%

    Purpose

    Topical Analgesic

  • Uses:

    • For the temporary relief of pain.
  • Warnings:

    not intended for ingestion. For external use only

    Do not use

    • in large quantities, Particularly over raw surfaces, or blistered areas.

    When using this product

    • Avoid contact with the eyes.

    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.

    Keep out of reach of children.

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

    If pregnant or breast-feeding,

    ask a health professional before use.

  • Directions:

    • Adults and children 2 years of age and older:Apply to affected area not more than 3 to 4 times daily.
    • Children under 2 years of age: consult a doctor.
  • Other information:

    • Store at 20-25°C (68-77°F) and protect from moisture.
  • Inactive ingredients:

    ALoe Barbadensis Leaf (Aloe Vera Gel) JUice, Aqua (Deionized Water), Calendula Officinalis Extract, Chamomilla Matricaria (Chamomile) Extract,Cyanocobalimin (Vitamin B 12), Ethylhexylglycerin, Ethyl Vanillin, Glycerin, Phenoxyethanol, Polysorbate-20, Pyridoxine HCL (Vitamib B6), SD-Alcohol 40B, Sodium Metabisulfite, Tetrasodium EDTA, Zemea (Corn) Propanediol

  • Questions?

    1-800-272-1875 / www.hennikahealth .com

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    LIDOSOLVE PAIN RELIEF 
    lidocaine hydrochloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83646-420
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE40 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
    CHAMOMILE (UNII: FGL3685T2X)  
    CYANOCOBALAMIN (UNII: P6YC3EG204)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    ETHYL VANILLIN (UNII: YC9ST449YJ)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)  
    SODIUM METABISULFITE (UNII: 4VON5FNS3C)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    CORN (UNII: 0N8672707O)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83646-420-00170 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/22/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01705/22/2023
    Labeler - HENNIKA HEALTH, LLC (118847402)
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