Label: RAPID PAIN-RELIEF TOPICAL- lidocaine hydrochloride, menthol cream

  • NDC Code(s): 82798-295-02, 82798-295-06
  • Packager: NORDIC HEALTHY LIVING INC.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 6, 2023

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  • Drug Facts

  • Active ingredients

    Lidocaine HCL 4.00% Menthol 1.00%

    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 raw surfaces or blistered areas. 

    When using this product

    • Avoid contact with 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), Arnica Montana Flower Extract, Ascorbic Acid (Vitamin C), Boswellia Serrata Extract, Caprylic/Capric Triglyceride, Carbomer, Ceteareth-20, Cetearyl Alcohol, Cetyl Alcohol, Ethylhexylglycerin, Glycerin, Ilex Paraguariensis (Yerba Mate’) Extract, Magnesium Sulfate, Methylsulfonylmethane (MSM), Methyl salicylate, Phenoxyethanol, Potassium Hydroxide.

  • Questions?

    (800) 564-1408

  • Package Labeling: RAPID PAIN-RELIEF TOPICAL CREAM, 2oz/60ml

    Label01

  • Package Labeling: RAPID PAIN-RELIEF TOPICAL CREAM, 6oz/175ml

    Label02

  • INGREDIENTS AND APPEARANCE
    RAPID PAIN-RELIEF TOPICAL 
    lidocaine hydrochloride, menthol cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82798-295
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE40 mg  in 1 mL
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL10 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)  
    MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    METHYL SALICYLATE (UNII: LAV5U5022Y)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82798-295-0260 mL in 1 TUBE; Type 0: Not a Combination Product07/01/2022
    2NDC:82798-295-06175 mL in 1 TUBE; Type 0: Not a Combination Product07/01/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01707/01/2022
    Labeler - NORDIC HEALTHY LIVING INC. (118546272)
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