Active Ingredient
Ethyl alcohol 70%
Hand Sanitizer
FDA Label NDC 78025-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Le Chandelle for the product Hand Sanitizer (NDC 78025-001). 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 active ingredient, purpose, uses, warnings, otc - do not use, stop use and ask a doctor, when using this product., 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
Purpose
Antiseptic
Uses
- for handwashing to decrease bacteria on the skin.
Warnings
For external use only-hands Flammable.Keep away from heat and flame.
Otc - Do Not Use
- if skin irritation develops
Stop Use And Ask A Doctor
if skin irritation develops
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.
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 above105℉
- may discolor some fabrics
- harmful to wood finishes and plastics
Inactive Ingredients
Water,Aloe Barbadensis Leaf Extract, Acrylates Copolymer,Triethanolamine,Tocopherly Acetate,Glycerin,
Jojoba Wax PEG-120 Esters,Citral,Citronellol,Geraniol,Limonene,Linalool,Fragrance
Package Label,Principal Display Panel
60ml Label (Label1)
100ml Label (Label2)
* Please review the disclaimer below.
