Active Ingredient
Alcohol 70%
She Elizabeth Bio Hand Sanitizer
FDA Label NDC 79487-010
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Liz Corporation Ltd for the product She Elizabeth Bio Hand Sanitizer (NDC 79487-010). 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, inactive ingredients, purpose, warnings, keep out of reach of children, uses, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredients
Water, Butylene Glycol, Carbomer, Triethanolamine, Aloe Barbadensis Leaf Extract, Artemisia Vulgaris Extract
Purpose
Antiseptic
Warnings
For external use only. Flammable. Keep away from heat and 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 skin irritation or rash develops.
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Uses
Hand sanitizer to decrease bacteria on the skin that could cause disease
Directions
■ Place enough product on hands to cover all surfaces. Rub hands together until dry.
■ Supervise children under 6 years of age when using this product to avoid swallowing.
Other Information
• Store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)
Questions?
+82-31-283-2233 or visit http://www.sheliz.com
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