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

NeuroRescueX HH333 by

Drug Labeling and Warnings

NeuroRescueX HH333 by is a Otc medication manufactured, distributed, or labeled by Panacura Inc., KyungJin Pharm.co.,Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

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

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84074-001
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S) (SCUTELLARIA BAICALENSIS ROOT - UNII:7J95K7ID2S)	SCUTELLARIA BAICALENSIS ROOT	240 mg
COPTIS JAPONICA ROOT (UNII: JH0SWT16D1) (COPTIS JAPONICA ROOT - UNII:JH0SWT16D1)	COPTIS JAPONICA ROOT	240 mg
PHELLODENDRON CHINENSIS BARK (UNII: 2866QMZ434) (PHELLODENDRON CHINENSIS BARK - UNII:2866QMZ434)	PHELLODENDRON CHINENSIS BARK	240 mg
GARDENIA JASMINOIDES FRUIT (UNII: 7CTH8MD549) (GARDENIA JASMINOIDES FRUIT - UNII:7CTH8MD549)	GARDENIA JASMINOIDES FRUIT	240 mg
RHEUM PALMATUM ROOT (UNII: G025DAL7CE) (RHEUM PALMATUM ROOT - UNII:G025DAL7CE)	RHEUM PALMATUM ROOT	60 mg

Inactive Ingredients
Ingredient Name	Strength
STARCH, CORN (UNII: O8232NY3SJ)
MAGNESIUM STEARATE (UNII: 70097M6I30)
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)

Product Characteristics
Color	yellow	Score	no score
Shape	CAPSULE	Size	21mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84074-001-03	2 in 1 CARTON	12/08/2025
1	NDC: 84074-001-02	6 in 1 CARTON
1	NDC: 84074-001-01	10 in 1 BLISTER PACK; Type 0: Not a Combination Product
2	NDC: 84074-001-05	3 in 1 CARTON	12/08/2025
2	NDC: 84074-001-04	10 in 1 BLISTER PACK; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/05/2024

Labeler - Panacura Inc. (695390655)

Registrant - Panacura Inc. (695390655)

Establishment
Name	Address	ID/FEI	Business Operations
KyungJin Pharm.co.,Ltd		695542024	manufacture(84074-001)