Nano Pure
FDA Label NDC 71530-026

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Nano Global for the product Nano Pure (NDC 71530-026). 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 ingredients, purpose, uses, warnings, do not use, ask a doctor before use if you have, stop use and ask a doctor if, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredients

Benzalkonium Chloride 0.10%

Purpose

Antiseptic

Uses

• Helps reduce bacteria on skin that potentially cause disease.

Warnings

For external use only.

Do Not Use

• in the eyes; if contact occurs, rinse thoroughly with water.

• over large areas of the body.

• if you are allergic to any ingredients.

Ask A Doctor Before Use If You Have

• deep puncture wounds.

• animal bites.

• serious burns.

Stop Use And Ask A Doctor If

• condition persists or gets worse.

• skin irritation or redness develop.

Keep Out Of Reach Of Children.

• In case of accidental ingestion, get medical help or contact Poison Control Center immediately.

Directions

•Spray onto hands or skin and apply evenly until dry.

Other Information

• Store at 15° to 30°C (59° to 86°F). Avoid freezing and excessive heat above 40°C (104°F)

Inactive Ingredients

1-Octadecanaminium,N,N-dimethyl-N(3-(trihydroxysilyl)-propyl)-chloride, Ethyl Alcohol, Fragrance (Parfum), Purified Water.

Questions?

1-833-777-NANO

* Please review the disclaimer below.