Pureus
FDA Label NDC 78286-306

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Winmedia24 for the product Pureus (NDC 78286-306). 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 drug facts, active ingredients, purpose, warnings, directions, inactive ingredients, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Drug Facts

Active Ingredients

Alkyl-C12-C16-Dimethyl-Benzyl Chloride Dihydrate

Purpose

Antimicrobial

Warnings

Flammable, Keep away from fire and flames

For External use only

When using this product

▪ do not get into eyes
▪ if contact occurs, rinse eyes thoroughly with water

Stop use and ask a doctor if

▪ irritation and redness develop

Directions

▪ wet hands thoroughly with product and allow to dry without wiping

Inactive Ingredients

Distilled water, Glycerine, Vitamin E, Lemon Essential Oil

Packaging

Image (Label306)

Image (Label306)

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