Adirondack Botanical Organics Hand Sanitizer
FDA Label NDC 80987-000
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Blue Ocean Tech Llc for the product Adirondack Botanical Organics Hand Sanitizer (NDC 80987-000). 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 ingredients, purpose, use, warnings, do not use, keep out of reach of children., stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients
Ethyl Alcohol 77% v/v
Purpose
Anti-Microbial
Use
Hand sanitizer to reduce microbial contamination.
Warnings
Flammable. Keep away from fire or flame. Store below 110°F (43°C). Do not leave in or on hot surfaces. Do not leave in auto or any heated area. For external use only.
Do Not Use
in or near eyes. If in contact with eyes rinse eyes thoroughly with water.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a poison control center.
Stop Use
immediately if irritation or rash appears and lasts seek medical attention. Not for internal use.
Directions
Spray on hands. Rub into hands thoroughly. Children under 8 should be supervised when uing this product.
Other Ingredients
Water, Witch Hazel, Aloe Barbadenis Apinol.
Package Labeling:
55.15 mL (Package)
* Please review the disclaimer below.
