Otc - Active Ingredient
Active Ingredient:
Ethyl Alcohol 62%
Hand Sanitizer
FDA Label NDC 71828-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Wag Labs, Inc. for the product Hand Sanitizer (NDC 71828-001). 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 otc - active ingredient, otc - purpose, warnings, otc - stop use, otc - keep out of reach of children, dosage & administration, inactive ingredient, other safety information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose
Antibacterial
Warnings
Warnings
Flammable. Keep away from fire or flame.
For external use only.
Otc - Stop Use
Stop use and ask a doctor if irritation or rash develops and continues for more that 72 hours.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact your Poison Control Center right away.
Dosage & Administration
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.
Inactive Ingredient
Inactive Ingredients
Water, Aloe Barbadensis Leaf Juice, Maltodextrin, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanoamine
Other Safety Information
Other Information
Do not store above 105F. May discolor some fabrics. Harmful to wood finishes and plastics
Indications & Usage
Uses
For hand washing to decrease bacteria on the skin. Recommended for repeated use.
Otc - When Using
When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
* Please review the disclaimer below.
