Active Ingredient
Alcohol 75%
Hand Sanitizer
FDA Label NDC 76546-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Southern Telecom, Inc. for the product Hand Sanitizer (NDC 76546-001). 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, use, warnings, do not use, 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
Use
Hand sanitizer to help reduce bacteria on the skin.
Warnings
Flammable. Keep away from fire or flame.
For external use only, do not inhale or ingest.
Do Not Use
in, or near the eyes. In case of contact with eyes, rinse thoroughly with water.
Avoid contact with broken skin
Stop Use And Ask A Doctor If
redness or irritation develops, irritation or rash develop and persist for more than 72 hours.
Keep Out Of Reach Of Children
if swallowed, get medical help or contact a Poison Control Center immediately.
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
- Store below 110°F (43°C)
- May discolor certain fabrics or surfaces
Inactive Ingredients
Water, Triethanolamine, Carbomer, Aloe Vera Gel, Fragrance, Glycerin, Propylene Glycol
Package Label
Package Label (Cleanologyhndsntzr75)
* Please review the disclaimer below.
