NeuroRescueX HH333

Manufacturer
Panacura Inc. | KyungJin Pharm.co.,Ltd
Effective date
2025-12-09
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-06-01 01:21:20

Label at a glance#

ProductNeuroRescueX HH333
Active ingredientSCUTELLARIA BAICALENSIS ROOT, COPTIS JAPONICA ROOT, PHELLODENDRON CHINENSIS BARK, GARDENIA JASMINOIDES FRUIT, RHEUM PALMATUM ROOT
Label structure13 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

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

OTC - ACTIVE INGREDIENT SECTION

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) 

OTC - PURPOSE SECTION

prevention of cerebrovascular diseases, cardiovascular disease

OTC - DO NOT USE SECTION

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

OTC - ASK DOCTOR SECTION

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 SECTION

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

WARNINGS SECTION

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

OTC - STOP USE SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of the children.

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84074-001-01NeuroRescueX HH33310 in 1 BLISTER PACKCAPSULE109
84074-001-02NeuroRescueX HH3336 in 1 CARTONCAPSULE69
84074-001-03NeuroRescueX HH3332 in 1 CARTONCAPSULE29
84074-001-04NeuroRescueX HH33310 in 1 BLISTER PACKCAPSULE109
84074-001-05NeuroRescueX HH3333 in 1 CARTONCAPSULE39

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84074-00184074-001-01, 84074-001-02, 84074-001-03, 84074-001-04, 84074-001-05

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
82025-10-31monthly-update2026-06-03 17:38:34
72024-05-09full-release2026-06-01 00:12:21

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
NeuroRescueX HH333SCUTELLARIA BAICALENSIS ROOT, COPTIS JAPONICA ROOT, PHELLODENDRON CHINENSIS BARK, GARDENIA JASMINOIDES FRUIT, RHEUM PALMATUM ROOTPanacura Inc.7fc6fed4-6604-43ca-8850-1a594b64eaa52025-12-09WarningsExact identifier
ndc (package): 84074-001-02
ndc (package): 84074-001-03
ndc (package): 84074-001-01
ndc (package): 84074-001-05
ndc (package): 84074-001-04
ndc (product): 84074-001
ndc11 (package): 84074000105
ndc11 (package): 84074000104
ndc11 (package): 84074000102
ndc11 (package): 84074000103
ndc11 (package): 84074000101
spl id: 45839b43-a4c2-2ef6-e063-6294a90a9743
spl set id: 7fc6fed4-6604-43ca-8850-1a594b64eaa5

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.