Label: SHINGBASE TOPICAL ANALGESIC- lidocaine, menthol cream

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

Drug Label Information

Updated February 19, 2024

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  • Drug Facts

  • Active ingredients

    Lidocaine 4%

    Menthol 1%

    Purpose

    Topical Analgesic

  • Indications:

    Temporary relieves minor pain

  • Warnings:

    Avoid contact with the eyes. If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a physician

    • Do not apply to wounds or damaged skin.
    • Do not bandage tightly.

    Do not use

    in large quantities, particularly over raw surfaces or blistered areas.

    Keep out of reach of children to avoid accidental ingestion!

    If swallowed, get medical help or contact the poison control center immediately.

  • Directions:

    • use only as directed 
    • adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily
    • children under 12 years of age: consult a doctor
  • Other Information:

    Store at 20 to 25 C (68 to 77F)

  • Inactive Ingredients:

    L-arginine, Sodium Benzonate, Rectified Spirit, Disodium EDTA, Phenoxyetanol, Polysorbate 20, DM Water

  • Package Labeling:

    Bottle

  • INGREDIENTS AND APPEARANCE
    SHINGBASE TOPICAL ANALGESIC 
    lidocaine, menthol cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80327-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE40 mg  in 1 g
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL10 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ARGININE (UNII: 94ZLA3W45F)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80327-002-01120 g in 1 BOTTLE; Type 0: Not a Combination Product09/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01709/01/2020
    Labeler - JOONEM LLC (117633878)
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