Sealuxe Hand Sanitizer
FDA Label NDC 79959-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Apr Beauty Group Inc. for the product Sealuxe Hand Sanitizer (NDC 79959-001). 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 other, active ingredient, purpose, uses, warnings, otc - when using, otc - stop use, otc - 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

Other

Drug Facts

Active Ingredient

Ethyl Alcohol, 70% w/w 

Purpose

Antiseptic

Uses

Kills harmful bacteria/germs

Warnings

 Flammable, keep away from open flame and sources of  heat.

Otc - When Using

For occasional and personal domestic use.

Otc - Stop Use

Stop use and consult a health care practitioner if irritation develops.

Avoid contact with eyes.

If contact occurs, rinse thoroughly with water.

Otc - Keep Out Of Reach Of Children

If swallowed, call a posion control centre.

Directions

Rub thoroughly into hands for at least 30 seconds until dry.

For children 2 years and over supervise when product is used 

Other Information

Recommended storage conditions:

20 Degress Celsius

Inactive Ingredients

 Aloe barbadensis leaf juice, Aminomethyl Propanol, Glycerin , Propylene Glycol, Water, Isopropyl Myristate,Carbomer

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