Purpose
Antiseptic
Anticeptic
Sanspray-na
FDA Label NDC 70445-606
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-na (NDC 70445-606). 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 purpose, warnings:, directions, inactive ingredient:, drug facts, 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
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.
Directions
Spray enough product on hands to cover
all surfaces. Rub hands together until dry.
Inactive Ingredient:
Water, Aloe Vera, Glycerin, Propylene Glycol, Tocopherol, Lemon Fragrance.
Drug Facts
Active Ingredient Purpose
Benzalkonium Chloride (0.1%)
Spray enough product on hands to cover
all surfaces. Rub hands together until dry.
Keep Out Of Reach Of Children
keep out of reach of children
Package Label.Principal Display Panel
Ssna (Ssna)
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