Label: POWERFULX GINSENG RECOVERYCREAM- panax ginseng root water, acetyl glucosamine, dimethyl sulfone cream

  • 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 7, 2021

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

  • ACTIVE INGREDIENT

    Panax Ginseng Root Water, Acetyl Glucosamine, Dimethyl Sulfone, Sodium Chondroitin Sulfate

  • INACTIVE INGREDIENT

    Water, etc

  • PURPOSE

    Massage and Recovery cream

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children


  • WARNINGS

    Consult a physician if you have any abnormal symptoms such as red spots, swelling or itching, or side effects caused by direct sunlight.

  • DOSAGE & ADMINISTRATION

    for external use only


  • INDICATIONS & USAGE

    Apply a proper amount of this product to skin 10 minutes before exercise.

    After shower, apply to skin and massage.

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    POWERFULX GINSENG RECOVERYCREAM 
    panax ginseng root water, acetyl glucosamine, dimethyl sulfone cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70042-0004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) (DIMETHYL SULFONE - UNII:9H4PO4Z4FT) DIMETHYL SULFONE0.1 g  in 100 mL
    N-ACETYLGLUCOSAMINE (UNII: V956696549) (N-ACETYLGLUCOSAMINE - UNII:V956696549) N-ACETYLGLUCOSAMINE0.15 g  in 100 mL
    PANAX GINSENG ROOT WATER (UNII: P9T4K47OM0) (PANAX GINSENG ROOT WATER - UNII:P9T4K47OM0) PANAX GINSENG ROOT WATER66.2186 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70042-0004-12 mL in 1 POUCH; Type 0: Not a Combination Product12/10/2018
    2NDC:70042-0004-2500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product12/10/2018
    3NDC:70042-0004-3600 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product12/10/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other12/10/2018
    Labeler - Powerful X (689515038)
    Registrant - Powerful X (689515038)
    Establishment
    NameAddressID/FEIBusiness Operations
    Powerful X689515038manufacture(70042-0004) , label(70042-0004) , pack(70042-0004)