Antibacterial Foaming Hand Sanitizer
FDA Label NDC 72102-056

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Maketa,llc for the product Antibacterial Foaming Hand Sanitizer (NDC 72102-056). 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 ingredients, purpose, uses, warnings, otc - do not use, 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.

Other

Drug Facts

Active Ingredients

Benzalkonium Chloride

Purpose

Antimicrobial

Uses

Sanitizes hands to help reduce bacteria that potentially cause diseases.

Warnings

For External use only. Use on hands only. Do not use over large areas of the body.

Otc - Do Not Use

Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.

Otc - Stop Use

Stop Use and ask a doctor if irritation and redness develops , or persist for more than 72 hours.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children

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

Directions

Place enough product in your palm to thoroughly cover your hands. Rub hands together briskly until hands are entirely dry.

Other Information

Store at room temperature.

Inactive Ingredients

Leaf Juice, Water, Glycerin, Aloe Barbadensis Bisabolol , PEG-8, Disodium EDTA, Polysorbate-20, PEG-40, Sorbitan Peroleate, Allantoin, Sodium Benzoate, Fragrance

Questions?

(800) 638-8149

Principal Display Panel - 281 Ml Bottle Label

Makéta™

antimicrobial
FOAMING HAND
SANITIZER

kills 99.99%
of all germs

9.5 fl. oz. (281 ml)

Principal Display Panel (281 ml Bottle Label)

Principal Display Panel (281 ml Bottle Label)

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