FDA Label for Sanspray
View Indications, Usage & Precautions
Sanspray Product Label
The following document was submitted to the FDA by the labeler of this product Beacon Promotions 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.
Drug Facts
Ethyl Alcohol (62%)
Dosage & Administration
Ethyl Alcohol (62%)
Spray enough product on hands to cover
all surfaces. Rub hands together until dry.
Inactive Ingredients
Deionized Water, Glycerin, Propylene Glycol, Tocopherol, Fragrance, Aloe Vera.
Purpose
Antiseptic
Anticeptic
Directions
Spray enough product on hands to cover
all surfaces. Rub hands together until dry.
Warnings
For external use only. Flammable. Keep away from heat or flame. Keep out of eyes, ears
& mouth. In case of contact with eyes, rinse eyes thoroughly with water. Stop use and ask doctor if
redness or irritation develop and persist for more than 72 hours. Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.
Do not use on children less than 2 months of age. Do not use on open skin wounds.
Keep Out Of Reach Of Children
Keep out of reach of children
Package Label.Principal Display Panel
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