Freshorize
FDA Label NDC 52305-200

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Freshorize, Ltd. for the product Freshorize (NDC 52305-200). 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 keep out of reach of children, purpose, dosage & administration, inactive ingredient, active ingredients, use information, warnings, display of package label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Keep Out Of Reach Of Children

Keep out of reach of children


Purpose

Kills 99.9% Bacteria


Dosage & Administration

Requires no water or towels.

Apply small amount to hands and rub lightly until dry.

Inactive Ingredient

Alcohol denat, Aqua, acrylates/C10-30 alkyl, acrylate cross polymer, triethanolamine (TEA), parfum

Active Ingredients

62.5% Ethyl Alcohol.

Use Information

Requires no water or towels.  Apply small amount to hands and rub lightly until dry.

Warnings

Safety: For External Use Only.Use on Hands only.

Flammable.  Keep away from  fire or flame.

Avoid contact with  Eyes, should this occur  rinse immediately with clean warm water.

Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours.

Keep out of reach of children.

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

Display Of Package Label


Image Of Display (Freshorize Alc Based Label)

Image Of Display (Freshorize Alc Based Label)


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