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Drug Facts
Dist. by UPI, Atlanta, GA 30326 USA
Topsani
FDA Label NDC 24439-321
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by United Promotions Inc. for the product Topsani (NDC 24439-321). 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 other, active ingredients, purpose, indications, warning, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients
Benzalkonium Chloride 0.125%
Purpose
Antimicrobial
Indications
For handwashing to decrease bacteria on the skin.
Warning
For external use only.
Otc - When Using
When using this product avoid contact with the eyes. Rinse with water to remove.
Otc - Stop Use
Stop use and ask a doctor if rash or irritation develops and lasts.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed get medical help or contact a poison control center right away.
Directions
Wet hands thoroughly with product and allow to dry without wiping.
Inactive Ingredients
Blue 1, Fragrance, Hydroxypropyl Methylcellulose, Polysorbate-20, SD Alcohol 40-B, Urea, Water
Questions Or Comments?
Call 1-877-541-6055
Principal Display Panel - 56 Ml Bottle Label
non-alcohol based
PronTech™
Technology
topsani
HAND SANITIZER + MOISTURIZER
Lasting Anti-Bacterial Protection
KILLS 99.999%
of microorganisms
all you
need is a
dimesize
drop
2 FL OZ (56 mL)
Principal Display Panel (56 mL Bottle Label)
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