Active Ingredient
HOVENIA DULCIS THUNB. 19%
Reset U
FDA Label NDC 82229-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Doctor Care for the product Reset U (NDC 82229-001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, uses, when using this product,, stop use and ask a doctor if, keep out of reach of children, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Hangover
Uses
Helps relieve headache, fatigue, nausea, vomiting caused from consumption of alcohol
When Using This Product,
do not exceed recommended dosage
Stop Use And Ask A Doctor If
symptoms last for more than 2 weeks
Keep Out Of Reach Of Children
In case of overdose, get medical help or contact a Poison Control Center right away.
Directions
Drink one bottle a day.
Other Information
Store at room temperature
Inactive Ingredients
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
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