Active Ingredients
Ethyl Alcohol 70%
Instant Hand Sanitizer Spray
FDA Label NDC 73145-010
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Asc Marketing Ltd for the product Instant Hand Sanitizer (NDC 73145-010). 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 ingredients, purpose, use, warnings, do not use, keep out of reach of children., directions:, inactive ingredients:, 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.
Warnings
Flammable. Keep away from fire and flame.For external use only.
Do Not Use
in the eyes. In case of contact, rinse eyes thoroughly with water. Discontinue use if irritation and redness develop. If condition persists for more than 72 hours consult a doctor.
Keep Out Of Reach Of Children.
If swallowed get medical help or contact Poison Control Center right away.
Directions:
Wet hands thoroughly with product and allow to dry without wiping.
Inactive Ingredients:
Water, Glycerin, Propylene Glycol, Fragrance, Aloe Barbadensis Leaf Juice, Maltodextrin.
Package Labeling:
Label3 (Label3)
* Please review the disclaimer below.
