Active Ingredient
HOVENIA DULCIS THUNB. 19%
Miraculous Hangover
FDA Label NDC 82672-301
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Qingdao Aolixin Sanitary Products Co., Ltd. for the product Miraculous Hangover (NDC 82672-301). 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, do not use, when using this product, stop us and ask a doctor if, keep out of the reach of children, warnings, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Relieves symptoms of hangover
Uses
Helps relieve headache, fatigue, nausea, vomiting caused from consumption of alcohol
Do Not Use
If you are allergic to any ingredients of this product.
When Using This Product
Do not exceed recommended dosage
Stop Us And Ask A Doctor If
symptoms last for more than 2 weeks
Keep Out Of The Reach Of Children
Keep out of the reach of children
Warnings
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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