Alcohol Free Hand Sanitizer
FDA Label NDC 47993-231

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Ningbo Jiangbei Ocean Star Trading Co.,ltd for the product Alcohol Free Hand Sanitizer (NDC 47993-231). 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, indications & usage, dosage & administration, otc - keep out of reach of children, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

Active ingredients--------------purpose

Benzalkonium Chloride..........0.3%

Otc - Purpose

Uses:
Keep skin Clean. Recommended for repeated use.

Warnings

Warnings:

For external use only.Keep out of eyes.In case of eye contact immediately flush with water,call a doctor.If swallowed call a doctor.

Indications & Usage

Directions:

Squeeze small amount in your palm and briskly rub hands together until dry.

Dosage & Administration

Other Information

Do not store above 110F(43C) May discolor certain fabric or surfaces. Harmful to wood finishes and plastics.


Otc - Keep Out Of Reach Of Children

Children under 6 years of age should be super vised when using this product.

Inactive Ingredient

Inactive Ingredients:

Water,Cellulose,Triethanolamine,Ethoxylated hydrogenated castor oil,Glycerine,Fragrance

* Please review the disclaimer below.