Label: MSM- methylsulfonylmethane tablet

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated January 24, 2019

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

  • INDICATIONS & USAGE

    Twice a Day, 2 Tablets Per Intake with Water

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • DOSAGE & ADMINISTRATION

    for oral use only

  • WARNINGS

    Do not use this product if the expiration date has passed

    Hypersensitive reactions may occur for people with special needs and/or allergies. Please check the ingredients before intake

    When opening the product and/or during intake, please be careful as you may get hurt from the packaging

    Avoid direct sunlight and humid areas. Store and distribute in a cool area.

  • PURPOSE

    protect and maintain overall human health

    Helps with arthritis, pain relief, inflammation, muscle pain and improves blood flow

  • INACTIVE INGREDIENT

    water

  • ACTIVE INGREDIENT

    Methylsulfonylmethane

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    MSM 
    methylsulfonylmethane tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70694-0003
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) (DIMETHYL SULFONE - UNII:9H4PO4Z4FT) DIMETHYL SULFONE0.51 g  in 0.51 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeOVALSize15mm
    FlavorImprint Code none
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70694-0003-1122.4 g in 1 BLISTER PACK; Type 0: Not a Combination Product01/24/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/24/2019
    Labeler - Inc MBG (688436167)
    Establishment
    NameAddressID/FEIBusiness Operations
    Inc MBG688436167manufacture(70694-0003)