Active Ingredient
Ethyl Alcohol 70% Purpose: Antiseptic
Hand Sanitizer
FDA Label NDC 79727-000
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Deltamed Supply, Llc for the product Hand Sanitizer (NDC 79727-000). 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, use, warnings, keep out of reach of children, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
Hand sanitizer to help reduce bacteria on the skin
Warnings
Flammable. Keep away from fire or flame.
This product is intended for external use only
When using this product, do not use in or near the eyes.
In case of contact, rinse eyes thoroughly with water.
Discontinue use if irritation or redness develops. If condition persists for more than 72 hours, consult a doctor.
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- Place enough in your palm to cover your hands
- Rub hands together briskly until dry
- Children under 6 years of age should be supervised when using this product.
Other Information
- Store below 110°F (43°C)
- May discolor certain fabrics or surfaces
Inactive Ingredients
Water, Isopropyl Alcohol, Carbomer and Triethanolamine
Package Label.Principal Display Panel
500 ml NDC: 79727-000-02
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