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.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- DOSAGE & ADMINISTRATION
- ACTIVE INGREDIENT
- PURPOSE
- DO NOT USE
-
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
- WARNINGS
-
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
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
NEURORESCUEX HH333
scutellaria baicalensis root, coptis japonica root, phellodendron chinensis bark, gardenia jasminoides fruit, rheum palmatum root capsuleProduct 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:84074-001-02 6 in 1 CARTON 05/05/2024 1 NDC:84074-001-01 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)