Disposable Hand Sanitizer
FDA Label NDC 76562-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Ningbo Qiyu Commodity Co., Ltd. for the product Disposable Hand Sanitizer (NDC 76562-001). 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, purpose, use, warnings, when using this product, discontinue use if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredient

Alcohol, 62% v/v

Purpose

Antiseptic

Use

Decreases bacteria on hands

Warnings

For external use only

Flammable, keep away from fire or flame

When Using This Product

keep out of eyes.

Discontinue Use If

irritation and redness develops. If condition persists for more than 72 hours consult a doctor.

Keep Out Of Reach Of Children.

if swallowed, get medical help or contact a Poison Control Center right away.

Directions

Place a 'palmful' of product in one hand. Spread on both hands and rub the skin until dry.

Other Information

To report a serious adverse reaction please write to Added Extras, 16# Yonghe Road, Beilun District, Ningbo City, Zhejiang Province, China

Inactive Ingredients

Aqua, Glycerin, carbomer, Triethanolamine, Fragrance.

Package Labeling:

Label2 (Label2)

Label2 (Label2)

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