Active Ingredient
Ethyl alcohol 75%
Purago Hand Sanitizer
FDA Label NDC 76812-004
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Puraall Llc for the product Purago Hand Sanitizer (NDC 76812-004). 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, purpose, uses, warnings, when using this product, stop use and ask a doctor if, 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
Purpose
Antiseptic
Uses
- to decrease bacteria on the skin that could cause disease
- recommended for repeated use
Warnings
For external use only: hands
Flammable, keep away from 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 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.
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
Inactive Ingredients
Water, Aloe Barbadensis Leaf Extract, Acrylate/C10-30 alkyl Acrylate Crosspolymer, Tetrahydroxypropyl Ethylenediamine
Other Information
- do not store above 105°F
- may discolor some fabrics
- harmful to wood finishes and plastics
Package Labeling:
Label5 (Label5)
* Please review the disclaimer below.
