Active Ingredient
ACTIVE INGREDIENT: ALCOHOL 70.0%
The 99.9 Percent Hand Sanitizer
FDA Label NDC 74080-030
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Bb & Co., Ltd. for the product The 99.9 Percent Hand Sanitizer (NDC 74080-030). 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 ingredient, purpose, keep out of reach of children, uses:, warnings, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
INACTIVE INGREDIENTS:
Water, Glycerin, Butylene Glycol, Aloe Barbadensis Leaf Extract, Carbomer, Triethanolamine, Calendula Officinalis Extract, Flavor
Purpose
PURPOSE: SANITIZER
Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Uses:
Uses : Hand sanitizer to help reduce bacteria on the skin.
Warnings
Warnings:
Flammable. Keep away from fire or flame.
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
Directions:
• Put enough product in your palm to cover hands and rub hands together briskly until dry.
• Children under 6 years of age should be supervised when using this product.
Other Information
Other Information:
• Store below 90°F(32°C)
• May discolor certain fabrics or surfaces
* Please review the disclaimer below.
