Drug Facts
Ethyl Alcohol (62%)
Sanspray
FDA Label NDC 70445-605
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Beacon Promotions Inc for the product Sanspray (NDC 70445-605). 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 drug facts, dosage & administration, inactive ingredients, purpose, directions, warnings, keep out of reach of children, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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
Package Label (Sanspray)
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