Active Ingredient
Ethyl Alcohol 75%v/v
Wave Hand Sanitizer
FDA Label NDC 78754-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by C & A Marketing, Inc. for the product Wave Hand Sanitizer (NDC 78754-002). 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, when using this product, stop use and ask a doctor, 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
Uses
For reducing bacteria on the skin.
Warnings
For external use only. Flammable. Keep away from heat or flame
When Using This Product
Avoid contact with eyes, and if eye contact occurs, flush thoroughly with water and seek medical advice
Stop Use And Ask A Doctor
if irritation or rash occurs. These may be the signs of a serious condition.
Keep Out Of Reach Of Children
In case of accidentail ingestion, contact a doctor or Poison Control Center immediately.
Directions
• Dispense into dry hands and rub until dry. • Children under 6 years of age should be supervised by an adult when using this product.
Other Information
• Store below 110°F (43°C) • May discolor certain fabrics or surfaces.
Inactive Ingredients
Carbomer, water
Package Label
Package Label (Caaogrndchnahndsntzralchl75)
* Please review the disclaimer below.
