Active Ingredient(S)
Ethyl Alcohol 75% v/v
Purelogic Hand Sanitizer French Lavender
FDA Label NDC 77731-034
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Argento Sc By Sicura Inc. for the product Purelogic Hand Sanitizer French Lavender (NDC 77731-034). 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 active ingredient(s), otc - purpose, use, warnings, when using this product, stop use and ask a doctor, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose:
Antimicrobial
Use
Decrease bacteria on skin that could cause diseases
Recommended for repeated use
Warnings
For external use only. Flammable, keep way from flame or fire
When Using This Product
When using this product, keep out of eyes. In case of contact with eyes, flush thoroughly with water
Do not ingest or inhale
Avoid contact with broken skin
Stop Use And Ask A Doctor
if irrigation and redness develop or if condition persists for more than 72 hours
Keep Out Of Reach Of Children
if swallowed,get medical help or contact a Poison Control Center immediately
Directions
- Spread product on hands thoroughly and allow to dry, do not wipe off
- For children under 6, use under adult supervision
- Not recommended for use with infants
Other Information
Do not store above 105F (40.6C)
May discolor some fabrics
Harmful to plastics and wood finishes
Inactive Ingredients
Purified water, Carbomer, Triethanolamine, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate (Vitamin E), Fragrance, Blue 1 (42090), Red 33 (CI17200)
Package Label.Principal Display Panel
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