FDA Label for Poxiezzz
View Indications, Usage & Precautions
Poxiezzz Product Label
The following document was submitted to the FDA by the labeler of this product Fortunique B.v.. 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.
Active Ingredients
Menthol 1%
Zinc Oxide 4%
Purpose
Topical Analgesic
Skin Protectant
Uses
For the temporary relief of pain and itching associated with minor skin irritations
Protects chafed skin
Warning
For external use only
When using this product
Avoid contact with eyes
Stop Use And Contact A Doctor If
Condition worsens .
Symptoms last more than 7 days or clear up and occur within a few days.
Not to be applied over deep a puncture wounds, infection or lacerations
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away
Directions
Not suitable for children under 2 years of age. Adults and children 2 years of age and older: Apply to affected area no more than 2 to 3 times daily. Shake well before use. Make sure the skin is clean and dry before spraying. Use a sweeping movement to spray-on the cream in a thin and uniform layer directly onto the affected skin. Use a spraying distance of approximately 2 to 3 inches. It is not necessary to rub the cream. When the skin is very sensitive, it is advised not to touch the skin too frequently.
Other Information
Store at room temperature bellow 77° F
Inactive Ingredients
Water (aqua)
Coco-Caprylate/Caprate
Glycerin
Cetearyl Alcohol
Cetearyl Glucoside
Alky-Alcohols
Alkyl Glucoside
Cocoglycerides
Caprylylglycol
Caprylhydroxamic Acid
Silica
Oleic Acid
Principle Display Panel.Bottle Spray 50 Ml
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