Humaste Hand Sanitizer
FDA Label NDC 78287-170
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Swanrose, Inc. for the product Humaste Hand Sanitizer (NDC 78287-170). 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 drug facts, active ingredient, purpose, uses, warnings, • keep out of reach of children., directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Ethyl Alcohol 73%
Purpose
Antimicrobial
Uses
• Hand sanitizer to reduce microorganisms on the skin.
• Use this product when soap and water are not available.
Warnings
• For external use only. • Avoid contact with eyes. If contact occurs, rinse thoroughly with water. • FLAMMABLE. This product contains ethyl alcohol.Keep away from sources of ignition. • Discontinue use if irritation or redness develops. • If irritation persists for more than 72 hours, consult a physician.
• Keep Out Of Reach Of Children.
• If swallowed, get medical help or contact a Poison Control Center right away.
Directions
• Read the entire label before using this product.
• Place enough product on your palm to thoroughly cover your hands.
• Rub hands together briskly until dry.
Inactive Ingredients
Deinoized water, Glycerol Oil, Carbopol, Triethanolamine
Packaging
Image (7828717008 1)
* Please review the disclaimer below.
