Active Ingredients
Ethyl Alcohol 62%
Hand Sanitizer Gel
FDA Label NDC 70412-191
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zhejiang Ayan Biotech Co.,ltd. for the product Hand Sanitizer (NDC 70412-191). 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, uses:, warnings:, other, when using this product, stop use and ask a doctor, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses:
For Hand Sanitizing
Warnings:
For external use only - hands.
Other
Flammable. Keep away from heat and flame.
When Using This Product
Keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest.
Stop Use And Ask A Doctor
if skin irritation develops.
Keep Out Of Reach Of Children.
If swallowed, get medical help or call a Poison Control Center right away.
Directions:
Wet hands thoroughly with a product and allow to dry without wiping. For children under 6 use only under adult Supervision. Not recommended for infants.
Other Information
Do not store above 105 o F. May discolor some fabrics. Harmful to wood finishes and plastics.
Inactive Ingredients:
Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl ACetate, Triethanomalime, Water.
Package Labeling: 70412-191-08
70412-191-08 (70412 191 08)
Package Labeling: 70412-191-16
70412-191-16 (70412 191 16)
* Please review the disclaimer below.
