Reset U

Manufacturer
DOCTOR CARE
Effective date
2023-11-17
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:02:26

Label at a glance#

ProductReset U
Active ingredientHOVENIA DULCIS WHOLE
Label structure10 sections

Indications and uses

Helps relieve headache, fatigue, nausea, vomiting caused from consumption of alcohol

Dosage and administration

Drink one bottle a day.

Storage and handling

Store at room temperature

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

HOVENIA DULCIS THUNB. 19%

Purpose

OTC - PURPOSE SECTION

Hangover

Uses

DOSAGE & ADMINISTRATION SECTION

Helps relieve headache, fatigue, nausea, vomiting caused from consumption of alcohol

When using this product,

OTC - WHEN USING SECTION

do not exceed recommended dosage

Stop use and ask a doctor if

OTC - STOP USE SECTION

symptoms last for more than 2 weeks

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

INDICATIONS & USAGE SECTION

Drink one bottle a day.

Other information

STORAGE AND HANDLING SECTION

Store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

PUERARIA MONTANA VAR. LOBATA ROOT, CRATAEGUS PINNATIFIDA WHOLE, CIRSIUM JAPONICUM WHOLE, CITRUS RETICULATA WHOLE, WOLFIPORIA COCOS WHOLE, ATRACTYLODES LANCEA ROOT, SCHISANDRA CHINENSIS WHOLE, RUBUS COREANUS WHOLE, ASTRAGALUS PROPINQUUS ROOT, ZIZIPHUS JUJUBA VAR. INERMIS WHOLE, GLYCYRRHIZA URALENSIS WHOLE, ARTEMISIA CAPILLARIS WHOLE, PRUNUS MUME FLOWER, NASHIPATI, FRUCTOOLIGOSACCHARIDE

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

82229-001-0182229-001-01

82229-001-0282229-001-02

82229-001-0382229-001-03

82229-001-0482229-001-04

82229-001-0582229-001-05

82229-001-0682229-001-06

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82229-001-01Reset U75 mL in 1 BOTTLE, GLASSLIQUID754
82229-001-02Reset U17 mL in 1 POUCHLIQUID174
82229-001-03Reset U20 mL in 1 POUCHLIQUID204
82229-001-04Reset U100 mL in 1 BOTTLE, GLASSLIQUID1004
82229-001-05Reset U110 mL in 1 BOTTLE, PLASTICLIQUID1104
82229-001-06Reset U120 mL in 1 BOTTLE, PLASTICLIQUID1204

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82229-001RESET U (HOVENIA DULCIS THUNB.) LIQUID [DOCTOR CARE]4Legacy NDC, 6 package rows20231118_cc180db0-f9f5-5341-e053-2995a90ae6b8.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82229-00182229-001-01, 82229-001-02, 82229-001-03, 82229-001-05, 82229-001-06, 82229-001-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Source Document#

Source XML

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
0a546bd3-cf4b-6626-e063-6394a90a8b98cc180db0-f9f5-5341-e053-2995a90ae6b82023-11-17WarningsExact identifier
spl id: 0a546bd3-cf4b-6626-e063-6394a90a8b98
spl set id: cc180db0-f9f5-5341-e053-2995a90ae6b8

Reported adverse events (FAERS/openFDA)#

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