Active Ingredient
Alcohol 62%
Beautaniq Beauty Hand Sanitizer Spray
FDA Label NDC 78768-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Crop Beauty Group Inc. for the product Beautaniq Beauty Hand Sanitizer (NDC 78768-001). 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, when using this product, 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
for hand-washing to decrease bacteria on the skin, only when water is not available.
Warnings
Flammable, keep away from fire and flames
For external use only
When Using This Product
- do not get into eyes.
- if contact occurs, rinse eyes thoroughly with water.
Stop Use And Ask A Doctor If
irritation and redness develop.
Keep Out Of Reach Of Children.
if swallowed, get medical help or contact a Poison Control Center right away.
Directions
wet hands thoroughly with product and allow to dry without wiping.
Other Information
- Store below 105 °F.
- May discolor some fabrics.
Inactive Ingredients
Water,Aloe Barbadensis Extract,Fragrance.
Package Labeling:
Bottle (Bottle)
* Please review the disclaimer below.
