Label: NEURACIN TOPICAL GEL- neuracin topical analgesic gel gel

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

Drug Label Information

Updated May 20, 2024

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  • Active Ingredients

    Camphor 4%

    Menthol 10%

    Methyl Salicylate 30%

  • Purpose

    Topical Analgesic

  • Uses

    Temporarily relieves minor pain associated with:

    • Arthritis
    • Simple Backache
    • Muscle Strains
    • Bruises
    • Muscle Sprains
  • Warnings

    For External use only

    When using this product

    • avoid contact with eyes and mucous membranes
    • do no apply to wounds or damaged skin
    • do not bandage tightly or use with a heating pad
    • use only as directed

    Stop use and ask a doctor if condition worsens; symptoms last more than 7 days or clear up and occur again within a few days

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help right away. If pregnant Or Breast-Feeding, Ask A Health Professional Before Use

  • Directions

    • Apply on affected area, not more than 3 to 4 times daily
    • Children under 12 years of age; consult a doctor

  • Other Information

    • Store at 20-25ºC (68-77ºF) Store away from heat
  • Inactive Ingredients

    Benzyl alcohol, Carbomer, Pemulen, Polysorbate 80, Purified Water, Triethanolamine

  • PRINCIPAL DISPLAY PANEL

    Questions or comments? Call 1-866-747-7365

    Neuracin Topical Analgesic Gel

    NDC 70512-104-60

    Qty 2oz (56.7G)

    Carton

  • INGREDIENTS AND APPEARANCE
    NEURACIN TOPICAL GEL 
    neuracin topical analgesic gel gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70512-104
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE300 mg  in 1 g
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)40 mg  in 1 g
    MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM100 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)  
    CARBOMER 940 (UNII: 4Q93RCW27E)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70512-104-601 in 1 CARTON05/24/2021
    156.7 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01705/24/2021
    Labeler - SOLA Pharmaceuticals (080121345)
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