Active Ingredient(S)
Ethyl Alcohol 80% V/V
Ziva Hand Sanitizer
FDA Label NDC 81450-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ziva Wetwipes Fzco for the product Ziva Hand Sanitizer (NDC 81450-001). 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(s), purpose, uses, warnings, directions, storage, inactive ingredients., product label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
Hand sanitizer gives protection from bacteria & germs. Use when soap and water are not available
Warnings
-For external use only.
-Flammable, keep away from the flames.
DO NOT USE
If irritation and skin redness develop.
On open skin wounds
When using this product keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask for a doctor Irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Squeeze thumbnail size amount of gel in your palm. Then briskly rub hands together until dry.
Storage
Store between 15°-30° C (59°-86° F)
Avoid freezing and excessive heat above 40° C (104° F)
Inactive Ingredients.
Aqua, Glycerin, Triethanolamine, Carbomer, Tocopheryl Acetate (Vitamin E), Aloe Barbadensis Leaf Juice.
Product Label
Image Description (Updated 001)
* Please review the disclaimer below.
