Lanco Antiseptic Hand Sanitizer
FDA Label NDC 80522-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Lanco Manufacturing, Corp. for the product Lanco Antiseptic Hand Sanitizer (NDC 80522-001). 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, active ingredient, purpose, uses, warnings, when using this product, stop use and ask a doctor if, 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 Ingredient
Ethyl alcohol 70%
Purpose
Antiseptic
Uses
- to decrease bacteria on the skin that could cause diseases
- Recommended for repeated use
Warnings
For external use only: hands
Flammable, keep away from heat, fire or flame.
When Using This Product
- keep out of eyes. In case of contact with eyes, flush thoroughly with water
- avoid contact with broken skin
- do not inhale or ingest
Stop Use And Ask A Doctor If
- Irritation and redness develop
- Condition persists for more than 72 hours
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
- for children under 6, use only under adult supervision
- not recommended for infants
Other Information
- do not Store above 105° F
- may discolor some fabrics
- harmful to wood finishes and plastics
Inactive Ingredients
water, glyceryl caprylate/caprate, glycerin, carboxyl vinyl polymer, propylene glycol, triethanolamine
Questions?
+1-787-736-4221
You may also report serious side effects to this phone number
Mon-Fri 9:00 AM - 5:00 PM
Package Labeling:
Bottle2 (Bottle2)
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