FDA Label for Hangover Relief
View Indications, Usage & Precautions
Hangover Relief Product Label
The following document was submitted to the FDA by the labeler of this product King Bio Inc.. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Otc - Active Ingredient
Drug Facts__________________________________________________________________________________________________________
HPUS activeingredients: Arsenicum album, Asarum europaeum, Avena sativa, Bryonia, Capsicum annuum, Carbo vegetabilis, Carboneum sulphuratum, Cinchona officinalis, Gelsemium sempervirens, Nux vomica, Paullinia sorbilis, Sulphuricum acidum. Equal volumes of each ingredient in 10X, 30X, LM1 potencies.
Indications & Usage
Uses for temporary relief of symptoms due to the over-consumption of alcohol: headache, nausea, vomiting, apathy, sensitivity to noise and light.
Inactive Ingredient
Inactive Ingredients: Bio-Energetically Enhanced™ pure water, citric acid and potassium sorbate.
Warnings
Warnings
- Stop use and ask your doctor, if symptoms persist or worsen.
- If pregnant or breast-feeding, ask a healthcare professional before use.
Otc - Keep Out Of Reach Of Children
- Keep out of reach of children
Dosage & Administration
Directions
- Initially, depress pump until primed.
- Spray one dose directly into mouth.
- Ages 12 and up: 3 sprays 3 times per day.
- Ages 2-12: 2 sprays 3 times per day.
Other Safety Information
Tamper resistant for your protection. Use only if safety seal is intact.
Otc - Purpose
Uses for temporary relief of symptoms due to the over-consumption of alcohol:
- headache
- nausea
- vomiting
- apathy
- sensitivity to noise and light.
Package Label.Principal Display Panel
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