Label: NEURORESCUEX HH333- scutellaria baicalensis root, coptis japonica root, phellodendron chinensis bark, gardenia jasminoides fruit, rheum palmatum root capsule

  • NDC Code(s): 84074-001-01, 84074-001-02
  • Packager: Panacura Inc.
  • 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 May 9, 2024

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

  • DOSAGE & ADMINISTRATION

    ■ For adults, take 2 capsules, once a day, ■ before or between meals

  • ACTIVE INGREDIENT

    Scutellaria Baicalensis Root (240 mg in 400 mg) 
    Coptis Japonica Root (240 mg in 400 mg) 
    Phellodendron Chinensis Bark (240 mg in 400 mg) 
    Gardenia Jasminoides Fruit (240 mg in 400 mg) 
    Rheum Palmatum Root (60 mg in 400 mg) 

  • PURPOSE

    prevention of cerebrovascular diseases, cardiovascular disease

  • DO NOT USE

    Do not use if you have
    ■ galactose intolerance
    ■ lapp lactase deficiency
    ■ glucose-galactose malabsorption (this medicine contains lactose)

  • ASK DOCTOR

    Ask a doctor before use if you are
    a patient with liver dysfunction (liver enzyme value (AST, ALT) levels more than 3 times normal)
    a patient who is being treated by a doctor or taking other medications.
    an elderly person (in general, elderly people should take with care, such as reducing their dosage, as their physiological function has deteriorated.)
    a child (the safety of children's use is not established. (Less experience in use))

  • INDICATIONS & USAGE

    ■ prevention of cerebrovascular diseases, cardiovascular disease
    ■ improvement of vascular endothelial cell function
    ■ adjunctive use to control hypertension, hyperlipidemia
    ■ weight loss support

  • WARNINGS

    Read the directions and warnings before use.
    KEEP THE PRODUCT INFORMATION. IT CONTAINS IMPORTANT INFORMATION.

  • STOP USE

    Stop use and ask a doctor, pharmacist or health professionals if
     There is no improvement of symptoms after taking it for a few days
     you have following symptoms after use
    ■ Skin trouble: ■ rash, ■ itch, ■ bloodshot, and etc.
    ■ Digestive system disorder: ■ anorexia, ■stomach discomfort, ■nausea, ■vomiting, and etc.
    ■ Liver disorder: ■ jaundice, ■ fatigue, and etc.
    ■ Interstitial lung disease: ■ difficult to breathe, ■ fever, and etc. accompanied by ■ cough.
    ■ Urinary system disorder: ■ dysuria
    ■ The autonomic system disorder: ■ insomnia, ■ excessive sweating, ■ fast pulse, ■frequent urination, ■ palpitations, ■ feeling helplessness, ■ excitement, and etc.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of the children.

  • INACTIVE INGREDIENT

    Corn Starch, Animal originated ingredients: Lactose Hydrate/ Magnesium Stearate

  • PRINCIPAL DISPLAY PANEL

    rescue

  • INGREDIENTS AND APPEARANCE
    NEURORESCUEX HH333 
    scutellaria baicalensis root, coptis japonica root, phellodendron chinensis bark, gardenia jasminoides fruit, rheum palmatum root capsule
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84074-001
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S) (SCUTELLARIA BAICALENSIS ROOT - UNII:7J95K7ID2S) SCUTELLARIA BAICALENSIS ROOT240 mg
    COPTIS JAPONICA ROOT (UNII: JH0SWT16D1) (COPTIS JAPONICA ROOT - UNII:JH0SWT16D1) COPTIS JAPONICA ROOT240 mg
    PHELLODENDRON CHINENSIS BARK (UNII: 2866QMZ434) (PHELLODENDRON CHINENSIS BARK - UNII:2866QMZ434) PHELLODENDRON CHINENSIS BARK240 mg
    GARDENIA JASMINOIDES FRUIT (UNII: 7CTH8MD549) (GARDENIA JASMINOIDES FRUIT - UNII:7CTH8MD549) GARDENIA JASMINOIDES FRUIT240 mg
    RHEUM PALMATUM ROOT (UNII: G025DAL7CE) (RHEUM PALMATUM ROOT - UNII:G025DAL7CE) RHEUM PALMATUM ROOT60 mg
    Inactive Ingredients
    Ingredient NameStrength
    STARCH, CORN (UNII: O8232NY3SJ)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    Product Characteristics
    ColoryellowScoreno score
    ShapeCAPSULESize21mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84074-001-026 in 1 CARTON05/05/2024
    1NDC:84074-001-0110 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/05/2024
    Labeler - Panacura Inc. (695390655)
    Registrant - Panacura Inc. (695390655)
    Establishment
    NameAddressID/FEIBusiness Operations
    KyungJin Pharm.co.,Ltd695542024manufacture(84074-001)