Label: ARTRIDON GLUCOSAMINE- menthol, methyl salicylate ointment

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

Drug Label Information

Updated October 29, 2024

If you are a consumer or patient please visit this version.

View All Sections
  • Drug Facts

  • Active Ingredients and Purpose

    Active ingredients

    		Purpose

    Menthol 2%...............................

    Topical analgesic

    Methyl Salicylate 15% ...............

    Topical analgesic

  • Uses

    For the temporary relief of minor aches and pains of muscles and joints associated with

    • simple backaches
    • arthritis
    • strains
    • bruises
    • sprains
  • Warnings

    For external use only. Avoid contact with the eyes.

    When using this product

    • do not apply on wounds or damaged skin
    • do not bandage tightly

    Stop use and ask a doctor if

    • condition worsens
    • symptoms persist for more than 7 days or clear up and occur again within a few days

    If pregnant or breast-feeding,

    ask a health professional before use.

    Keep out of reach of children.

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

  • 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: do not use, consult a doctor
  • Other information

    • store between 68-77°F (20-25°C)
    • don’t use if foil seal under cap is broken, torn, or missing
  • Inactive ingredients

    bromelains, cetyl alcohol, diazolidinyl urea, dimethicone, dimethyl sulfone, glucosamine, glycerin, isopropyl myristate, medium-chain triglycerides, mineral oil, potassium sorbate, propylene glycol, sorbic acid, xanthan gum, water

  • Dist by:

    PHARMADEL LLC

    New Castle, DE, 19720

    Questions? +1-866-359-3478

  • Principal Display Panel

    Artridon Glucosamina PDP

  • INGREDIENTS AND APPEARANCE
    ARTRIDON  GLUCOSAMINE
    menthol, methyl salicylate ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55758-030
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM2 g  in 100 g
    METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE15 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    GLUCOSAMINE (UNII: N08U5BOQ1K)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    BROMELAINS (UNII: U182GP2CF3)  
    SORBIC ACID (UNII: X045WJ989B)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    WATER (UNII: 059QF0KO0R)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55758-030-051 in 1 CARTON11/04/2024
    1142 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01711/04/2024
    Labeler - Pharmadel LLC (030129680)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!